Linked Data
ClinVar Variation Id:
2436358
ClinVar RCV Id:
RCV003138695
dbSNP Id:
rs773826036
ExAC:
1:158655070 A / G
gnomAD v2:
1-158655070-A-G
gnomAD v4:
1-158685280-A-G
COSMIC:
COSM315574
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.158685280A>G , CM000663.2:g.158685280A>G | GRCh38 |
| NC_000001.10:g.158655070A>G , CM000663.1:g.158655070A>G | GRCh37 |
| NC_000001.9:g.156921694A>G | NCBI36 |
| NG_011474.1:g.6437T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643759.2:c.92T>C MANE Select | ENSP00000495214.1:p.Val31Ala | |
| ENST00000368147.8:c.92T>C | ENSP00000357129.4:p.Val31Ala | |
| ENST00000467387.1:c.92T>C | ENSP00000476485.1:p.Val31Ala | |
| ENST00000614909.4:c.92T>C | ENSP00000482595.1:p.Val31Ala | |
| NM_003126.2:c.92T>C | NP_003117.2:p.Val31Ala | |
| XM_011509916.1:c.92T>C | XP_011508218.1:p.Val31Ala | |
| XM_011509917.1:c.92T>C | XP_011508219.1:p.Val31Ala | |
| XM_011509918.1:c.92T>C | XP_011508220.1:p.Val31Ala | |
| XM_011509919.1:c.92T>C | XP_011508221.1:p.Val31Ala | |
| XR_921911.1:n.205T>C | ||
| XR_921912.1:n.210T>C | ||
| NM_003126.3:c.92T>C | NP_003117.2:p.Val31Ala | |
| XM_011509916.2:c.92T>C | XP_011508218.1:p.Val31Ala | |
| XM_011509917.3:c.92T>C | XP_011508219.1:p.Val31Ala | |
| XM_011509918.3:c.92T>C | XP_011508220.1:p.Val31Ala | |
| XM_011509919.3:c.92T>C | XP_011508221.1:p.Val31Ala | |
| XR_921911.3:n.218T>C | ||
| XR_921912.2:n.220T>C | ||
| NM_003126.4:c.92T>C MANE Select | NP_003117.2:p.Val31Ala |