Linked Data
ClinVar Variation Id:
251764
dbSNP Id:
rs371355878
ExAC:
19:11224046 A / C
gnomAD v2:
19-11224046-A-C
gnomAD v3:
19-11113370-A-C
gnomAD v4:
19-11113370-A-C
PubMed:
PMID:26020417
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11113370A>C , CM000681.2:g.11113370A>C | GRCh38 |
| NC_000019.9:g.11224046A>C , CM000681.1:g.11224046A>C | GRCh37 |
| NC_000019.8:g.11085046A>C | NCBI36 |
| NG_009060.1:g.28990A>C , LRG_274:g.28990A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1537A>C | ENSP00000252444.6:p.Arg513= | |
| ENST00000559340.2:c.1279A>C | ENSP00000453696.2:p.Arg427= | |
| ENST00000560467.2:c.1159A>C | ENSP00000453513.2:p.Arg387= | |
| ENST00000558518.6:c.1279A>C MANE Select | ENSP00000454071.1:p.Arg427= | |
| ENST00000252444.9:c.1533A>C | ||
| ENST00000455727.6:c.775A>C | ENSP00000397829.2:p.Arg259= | |
| ENST00000535915.5:c.1156A>C | ENSP00000440520.1:p.Arg386= | |
| ENST00000545707.5:c.898A>C | ENSP00000437639.1:p.Arg300= | |
| ENST00000557933.5:c.1279A>C | ENSP00000453557.1:p.Arg427= | |
| ENST00000558013.5:c.1279A>C | ENSP00000453346.1:p.Arg427= | |
| ENST00000558518.5:c.1279A>C | ENSP00000454071.1:p.Arg427= | |
| ENST00000560173.1:n.278A>C | ||
| ENST00000560467.1:c.759A>C | ||
| NM_000527.4:c.1279A>C , LRG_274t1:c.1279A>C | NP_000518.1:p.Arg427= | |
| NM_001195798.1:c.1279A>C | NP_001182727.1:p.Arg427= | |
| NM_001195799.1:c.1156A>C | NP_001182728.1:p.Arg386= | |
| NM_001195800.1:c.775A>C | NP_001182729.1:p.Arg259= | |
| NM_001195803.1:c.898A>C | NP_001182732.1:p.Arg300= | |
| XM_011528010.1:c.1279A>C | XP_011526312.1:p.Arg427= | |
| XM_011528011.1:c.898A>C | XP_011526313.1:p.Arg300= | |
| XR_244074.2:n.1429A>C | ||
| XM_011528010.2:c.1279A>C | XP_011526312.1:p.Arg427= | |
| XR_001753685.2:n.1396A>C | ||
| XR_001753686.2:n.1396A>C | ||
| NM_000527.5:c.1279A>C MANE Select | NP_000518.1:p.Arg427= | |
| NM_001195798.2:c.1279A>C | NP_001182727.1:p.Arg427= | |
| NM_001195799.2:c.1156A>C | NP_001182728.1:p.Arg386= | |
| NM_001195800.2:c.775A>C | NP_001182729.1:p.Arg259= | |
| NM_001195803.2:c.898A>C | NP_001182732.1:p.Arg300= |