Linked Data
dbSNP Id:
rs749696264
ExAC:
15:40270284 C / T
gnomAD v2:
15-40270284-C-T
gnomAD v3:
15-39978083-C-T
gnomAD v4:
15-39978083-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.39978083C>T , CM000677.2:g.39978083C>T | GRCh38 |
| NC_000015.9:g.40270284C>T , CM000677.1:g.40270284C>T | GRCh37 |
| NC_000015.8:g.38057576C>T | NCBI36 |
| NG_034053.1:g.48960C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263791.10:c.2255C>T MANE Select | ENSP00000263791.5:p.Ala752Val | |
| ENST00000263791.9:c.2255C>T | ENSP00000263791.5:p.Ala752Val | |
| ENST00000560855.5:c.1671C>T | ||
| ENST00000624709.1:n.1105C>T | ||
| NM_001013703.3:c.2255C>T | NP_001013725.2:p.Ala752Val | |
| XM_005254392.1:c.2255C>T | XP_005254449.1:p.Ala752Val | |
| XM_011521599.1:c.2255C>T | XP_011519901.1:p.Ala752Val | |
| XM_011521600.1:c.2255C>T | XP_011519902.1:p.Ala752Val | |
| XM_005254392.3:c.2255C>T | XP_005254449.1:p.Ala752Val | |
| XM_011521599.2:c.2255C>T | XP_011519901.1:p.Ala752Val | |
| XM_011521600.3:c.2255C>T | XP_011519902.1:p.Ala752Val | |
| XM_017022219.2:c.2255C>T | XP_016877708.1:p.Ala752Val | |
| NM_001013703.4:c.2255C>T MANE Select | NP_001013725.2:p.Ala752Val |