Linked Data
ClinVar Variation Id:
2074191
ClinVar RCV Id:
RCV002976091
dbSNP Id:
rs1439801044
gnomAD v2:
12-125435336-G-A
gnomAD v4:
12-124950790-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.124950790G>A , CM000674.2:g.124950790G>A | GRCh38 |
| NC_000012.11:g.125435336G>A , CM000674.1:g.125435336G>A | GRCh37 |
| NC_000012.10:g.124001289G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308736.7:c.2883C>T MANE Select | ENSP00000311135.2:p.Asp961= | |
| ENST00000544745.2:c.2354C>T | ||
| ENST00000308736.6:c.2883C>T | ENSP00000311135.2:p.Asp961= | |
| ENST00000539298.1:n.2983C>T | ||
| ENST00000542400.5:n.1358C>T | ||
| ENST00000544745.1:c.2244C>T | ENSP00000439009.1:p.Asp748= | |
| NM_032656.3:c.2883C>T | NP_116045.2:p.Asp961= | |
| XM_005253590.2:c.2883C>T | XP_005253647.1:p.Asp961= | |
| XM_011538597.1:c.2883C>T | XP_011536899.1:p.Asp961= | |
| XM_005253590.3:c.2883C>T | XP_005253647.1:p.Asp961= | |
| XR_001748819.1:n.2986C>T | ||
| XR_001748820.1:n.2976C>T | ||
| NM_032656.4:c.2883C>T MANE Select | NP_116045.2:p.Asp961= |