Linked Data
dbSNP Id:
rs1645143168
gnomAD v4:
1-1047801-G-A
MyVariant Identifiers:
chr1:g.983181G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1047801G>A , CM000663.2:g.1047801G>A | GRCh38 |
| NC_000001.10:g.983181G>A , CM000663.1:g.983181G>A | GRCh37 |
| NC_000001.9:g.973044G>A | NCBI36 |
| NG_016346.1:g.32679G>A , LRG_198:g.32679G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379370.7:c.3657G>A MANE Select | ENSP00000368678.2:p.Val1219= | |
| ENST00000651234.1:c.3342G>A | ENSP00000499046.1:p.Val1114= | |
| ENST00000652369.1:c.3342G>A | ENSP00000498543.1:p.Val1114= | |
| ENST00000379370.6:c.3657G>A | ENSP00000368678.2:p.Val1219= | |
| ENST00000466223.1:n.395G>A | ||
| ENST00000478677.1:n.239G>A | ||
| ENST00000620552.4:c.3243G>A | ENSP00000484607.1:p.Val1081= | |
| NM_001305275.1:c.3657G>A | NP_001292204.1:p.Val1219= | |
| NM_198576.3:c.3657G>A | NP_940978.2:p.Val1219= | |
| XM_005244749.2:c.3657G>A | XP_005244806.1:p.Val1219= | |
| XM_006710635.2:c.3657G>A | XP_006710698.1:p.Val1219= | |
| XM_011541429.1:c.3657G>A | XP_011539731.1:p.Val1219= | |
| XM_011541430.1:c.2784G>A | XP_011539732.1:p.Val928= | |
| XM_011541431.1:c.1923G>A | XP_011539733.1:p.Val641= | |
| XR_946650.1:n.3724G>A | ||
| NM_001364727.1:c.3342G>A | NP_001351656.1:p.Val1114= | |
| XM_005244749.3:c.3657G>A | XP_005244806.1:p.Val1219= | |
| XM_011541429.2:c.3657G>A | XP_011539731.1:p.Val1219= | |
| XR_946650.2:n.3728G>A | ||
| NM_001305275.2:c.3657G>A | NP_001292204.1:p.Val1219= | |
| NM_198576.4:c.3657G>A MANE Select | NP_940978.2:p.Val1219= | |
| NM_001364727.2:c.3342G>A | NP_001351656.1:p.Val1114= |