Linked Data
dbSNP Id:
rs2150890965
gnomAD v4:
6-35456047-T-A
MyVariant Identifiers:
chr6:g.35423824T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35456047T>A , CM000668.2:g.35456047T>A | GRCh38 |
| NC_000006.11:g.35423824T>A , CM000668.1:g.35423824T>A | GRCh37 |
| NC_000006.10:g.35531802T>A | NCBI36 |
| NG_011708.1:g.8687T>A , LRG_498:g.8687T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696264.1:c.549T>A | ENSP00000512511.1:p.Ala183= | |
| ENST00000696265.1:c.549T>A | ENSP00000512512.1:p.Ala183= | |
| ENST00000696266.1:c.267T>A | ENSP00000512513.1:p.Ala89= | |
| ENST00000696267.1:n.189T>A | ||
| ENST00000229769.3:c.549T>A MANE Select | ENSP00000229769.2:p.Ala183= | |
| ENST00000648059.1:c.549T>A | ENSP00000497902.1:p.Ala183= | |
| ENST00000229769.2:c.549T>A | ENSP00000229769.2:p.Ala183= | |
| NM_021922.2:c.549T>A , LRG_498t1:c.549T>A | NP_068741.1:p.Ala183= | |
| XM_005248885.2:c.549T>A | XP_005248942.1:p.Ala183= | |
| XM_005248886.2:c.549T>A | XP_005248943.1:p.Ala183= | |
| XM_005248887.2:c.549T>A | XP_005248944.1:p.Ala183= | |
| XM_005248888.2:c.549T>A | XP_005248945.1:p.Ala183= | |
| XM_011514343.1:c.255T>A | XP_011512645.1:p.Ala85= | |
| XM_011514344.1:c.255T>A | XP_011512646.1:p.Ala85= | |
| XM_005248888.3:c.549T>A | XP_005248945.1:p.Ala183= | |
| XM_011514343.2:c.255T>A | XP_011512645.1:p.Ala85= | |
| XR_001743226.1:n.756T>A | ||
| XR_002956267.1:n.756T>A | ||
| NM_021922.3:c.549T>A MANE Select | NP_068741.1:p.Ala183= |