Linked Data
ClinVar Variation Id:
928433
ClinVar RCV Id:
RCV001192296
dbSNP Id:
rs746616623
gnomAD v4:
19-11129563-C-A
MyVariant Identifiers:
chr19:g.11240239C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11129563C>A , CM000681.2:g.11129563C>A | GRCh38 |
| NC_000019.9:g.11240239C>A , CM000681.1:g.11240239C>A | GRCh37 |
| NC_000019.8:g.11101239C>A | NCBI36 |
| NG_009060.1:g.45183C>A , LRG_274:g.45183C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2698C>A | ENSP00000252444.6:p.Arg900= | |
| ENST00000559340.2:c.*509C>A | ENSP00000453696.2:n.*509C>A | |
| ENST00000560467.2:c.2320C>A | ENSP00000453513.2:p.Arg774= | |
| ENST00000558518.6:c.2440C>A MANE Select | ENSP00000454071.1:p.Arg814= | |
| ENST00000252444.9:c.2694C>A | ||
| ENST00000455727.6:c.1936C>A | ENSP00000397829.2:p.Arg646= | |
| ENST00000535915.5:c.2317C>A | ENSP00000440520.1:p.Arg773= | |
| ENST00000545707.5:c.1906C>A | ENSP00000437639.1:p.Arg636= | |
| ENST00000557933.5:c.2502C>A | ENSP00000453557.1:p.Gly834= | |
| ENST00000558013.5:c.2440C>A | ENSP00000453346.1:p.Arg814= | |
| ENST00000558518.5:c.2440C>A | ENSP00000454071.1:p.Arg814= | |
| ENST00000560628.1:n.108+1909C>A | ||
| NM_000527.4:c.2440C>A , LRG_274t1:c.2440C>A | NP_000518.1:p.Arg814= | |
| NM_001195798.1:c.2440C>A | NP_001182727.1:p.Arg814= | |
| NM_001195799.1:c.2317C>A | NP_001182728.1:p.Arg773= | |
| NM_001195800.1:c.1936C>A | NP_001182729.1:p.Arg646= | |
| NM_001195803.1:c.1906C>A | NP_001182732.1:p.Arg636= | |
| XM_011528010.1:c.2362C>A | XP_011526312.1:p.Arg788= | |
| XM_011528011.1:c.2059C>A | XP_011526313.1:p.Arg687= | |
| XR_244074.2:n.2450C>A | ||
| XM_011528010.2:c.2362C>A | XP_011526312.1:p.Arg788= | |
| XR_001753685.2:n.2774C>A | ||
| XR_001753686.2:n.2417C>A | ||
| NM_000527.5:c.2440C>A MANE Select | NP_000518.1:p.Arg814= | |
| NM_001195798.2:c.2440C>A | NP_001182727.1:p.Arg814= | |
| NM_001195799.2:c.2317C>A | NP_001182728.1:p.Arg773= | |
| NM_001195800.2:c.1936C>A | NP_001182729.1:p.Arg646= | |
| NM_001195803.2:c.1906C>A | NP_001182732.1:p.Arg636= |