Linked Data
ClinVar Variation Id:
251551
ClinVar RCV Id:
RCV000238525
dbSNP Id:
rs879254733
PubMed:
PMID:20145306
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11110639T>A , CM000681.2:g.11110639T>A | GRCh38 |
| NC_000019.9:g.11221315T>A , CM000681.1:g.11221315T>A | GRCh37 |
| NC_000019.8:g.11082315T>A | NCBI36 |
| NG_009060.1:g.26259T>A , LRG_274:g.26259T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1199-13T>A | ENSP00000252444.6:n.1199-13T>A | |
| ENST00000559340.2:c.941-13T>A | ENSP00000453696.2:n.941-13T>A | |
| ENST00000560467.2:c.941-875T>A | ENSP00000453513.2:n.941-875T>A | |
| ENST00000558518.6:c.941-13T>A MANE Select | ENSP00000454071.1:n.941-13T>A | |
| ENST00000252444.9:c.1195-13T>A | ||
| ENST00000455727.6:c.437-13T>A | ENSP00000397829.2:n.437-13T>A | |
| ENST00000535915.5:c.818-13T>A | ENSP00000440520.1:n.818-13T>A | |
| ENST00000545707.5:c.560-13T>A | ENSP00000437639.1:n.560-13T>A | |
| ENST00000557933.5:c.941-13T>A | ENSP00000453557.1:n.941-13T>A | |
| ENST00000558013.5:c.941-13T>A | ENSP00000453346.1:n.941-13T>A | |
| ENST00000558518.5:c.941-13T>A | ENSP00000454071.1:n.941-13T>A | |
| ENST00000560467.1:c.541-875T>A | ||
| NM_000527.4:c.941-13T>A , LRG_274t1:c.941-13T>A | NP_000518.1:n.941-13T>A | |
| NM_001195798.1:c.941-13T>A | NP_001182727.1:n.941-13T>A | |
| NM_001195799.1:c.818-13T>A | NP_001182728.1:n.818-13T>A | |
| NM_001195800.1:c.437-13T>A | NP_001182729.1:n.437-13T>A | |
| NM_001195803.1:c.560-13T>A | NP_001182732.1:n.560-13T>A | |
| XM_011528010.1:c.941-13T>A | XP_011526312.1:n.941-13T>A | |
| XM_011528011.1:c.560-13T>A | XP_011526313.1:n.560-13T>A | |
| XR_244074.2:n.1091-13T>A | ||
| XM_011528010.2:c.941-13T>A | XP_011526312.1:n.941-13T>A | |
| XR_001753685.2:n.1058-13T>A | ||
| XR_001753686.2:n.1058-13T>A | ||
| NM_000527.5:c.941-13T>A MANE Select | NP_000518.1:n.941-13T>A | |
| NM_001195798.2:c.941-13T>A | NP_001182727.1:n.941-13T>A | |
| NM_001195799.2:c.818-13T>A | NP_001182728.1:n.818-13T>A | |
| NM_001195800.2:c.437-13T>A | NP_001182729.1:n.437-13T>A | |
| NM_001195803.2:c.560-13T>A | NP_001182732.1:n.560-13T>A |