SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-10-16T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
This migration is underway but taking longer than originally estimated.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
This migration is underway but taking longer than originally estimated.
Linked Data
ClinVar Variation Id:
251446
dbSNP Id:
rs200990725
ExAC:
19:11217315 C / T
gnomAD v2:
19-11217315-C-T
gnomAD v3:
19-11106639-C-T
gnomAD v4:
19-11106639-C-T
COSMIC:
COSM5498316
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11106639C>T , CM000681.2:g.11106639C>T | GRCh38 |
| NC_000019.9:g.11217315C>T , CM000681.1:g.11217315C>T | GRCh37 |
| NC_000019.8:g.11078315C>T | NCBI36 |
| NG_009060.1:g.22259C>T , LRG_274:g.22259C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1027C>T | ENSP00000252444.6:p.Arg343Trp | |
| ENST00000559340.2:c.769C>T | ENSP00000453696.2:p.Arg257Trp | |
| ENST00000560467.2:c.769C>T | ENSP00000453513.2:p.Arg257Trp | |
| ENST00000558518.6:c.769C>T MANE Select | ENSP00000454071.1:p.Arg257Trp | |
| ENST00000252444.9:c.1023C>T | ||
| ENST00000455727.6:c.314-753C>T | ENSP00000397829.2:n.314-753C>T | |
| ENST00000535915.5:c.646C>T | ENSP00000440520.1:p.Arg216Trp | |
| ENST00000545707.5:c.388C>T | ENSP00000437639.1:p.Arg130Trp | |
| ENST00000557933.5:c.769C>T | ENSP00000453557.1:p.Arg257Trp | |
| ENST00000558013.5:c.769C>T | ENSP00000453346.1:p.Arg257Trp | |
| ENST00000558518.5:c.769C>T | ENSP00000454071.1:p.Arg257Trp | |
| ENST00000558528.1:n.284C>T | ||
| ENST00000560467.1:c.369C>T | ||
| NM_000527.4:c.769C>T , LRG_274t1:c.769C>T | NP_000518.1:p.Arg257Trp | |
| NM_001195798.1:c.769C>T | NP_001182727.1:p.Arg257Trp | |
| NM_001195799.1:c.646C>T | NP_001182728.1:p.Arg216Trp | |
| NM_001195800.1:c.314-753C>T | NP_001182729.1:n.314-753C>T | |
| NM_001195803.1:c.388C>T | NP_001182732.1:p.Arg130Trp | |
| XM_011528010.1:c.769C>T | XP_011526312.1:p.Arg257Trp | |
| XM_011528011.1:c.388C>T | XP_011526313.1:p.Arg130Trp | |
| XR_244074.2:n.919C>T | ||
| XM_011528010.2:c.769C>T | XP_011526312.1:p.Arg257Trp | |
| XR_001753685.2:n.886C>T | ||
| XR_001753686.2:n.886C>T | ||
| NM_000527.5:c.769C>T MANE Select | NP_000518.1:p.Arg257Trp | |
| NM_001195798.2:c.769C>T | NP_001182727.1:p.Arg257Trp | |
| NM_001195799.2:c.646C>T | NP_001182728.1:p.Arg216Trp | |
| NM_001195800.2:c.314-753C>T | NP_001182729.1:n.314-753C>T | |
| NM_001195803.2:c.388C>T | NP_001182732.1:p.Arg130Trp |