Linked Data
ClinVar Variation Id:
1481092
ClinVar RCV Id:
RCV002022215
dbSNP Id:
rs755714257
ExAC:
8:87683186 G / A
gnomAD v2:
8-87683186-G-A
gnomAD v3:
8-86670958-G-A
gnomAD v4:
8-86670958-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86670958G>A , CM000670.2:g.86670958G>A | GRCh38 |
| NC_000008.10:g.87683186G>A , CM000670.1:g.87683186G>A | GRCh37 |
| NC_000008.9:g.87752302G>A | NCBI36 |
| NG_016980.1:g.77718C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.479C>T MANE Select | ENSP00000316605.5:p.Ala160Val | |
| ENST00000680314.1:n.240C>T | ||
| ENST00000681746.1:c.479C>T | ENSP00000505959.1:p.Ala160Val | |
| ENST00000320005.5:c.479C>T | ENSP00000316605.5:p.Ala160Val | |
| NM_019098.4:c.479C>T | NP_061971.3:p.Ala160Val | |
| XM_011517138.1:c.65C>T | XP_011515440.1:p.Ala22Val | |
| XM_011517138.2:c.65C>T | XP_011515440.1:p.Ala22Val | |
| NM_019098.5:c.479C>T MANE Select | NP_061971.3:p.Ala160Val |