Linked Data
ClinVar Variation Id:
1588453
ClinVar RCV Id:
RCV002096107
dbSNP Id:
rs1645019966
gnomAD v3:
1-1043971-C-T
gnomAD v4:
1-1043971-C-T
MyVariant Identifiers:
chr1:g.979351C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1043971C>T , CM000663.2:g.1043971C>T | GRCh38 |
| NC_000001.10:g.979351C>T , CM000663.1:g.979351C>T | GRCh37 |
| NC_000001.9:g.969214C>T | NCBI36 |
| NG_016346.1:g.28849C>T , LRG_198:g.28849C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379370.7:c.1947C>T MANE Select | ENSP00000368678.2:p.Ala649= | |
| ENST00000651234.1:c.1632C>T | ENSP00000499046.1:p.Ala544= | |
| ENST00000652369.1:c.1632C>T | ENSP00000498543.1:p.Ala544= | |
| ENST00000379370.6:c.1947C>T | ENSP00000368678.2:p.Ala649= | |
| ENST00000620552.4:c.1533C>T | ENSP00000484607.1:p.Ala511= | |
| NM_001305275.1:c.1947C>T | NP_001292204.1:p.Ala649= | |
| NM_198576.3:c.1947C>T | NP_940978.2:p.Ala649= | |
| XM_005244749.2:c.1947C>T | XP_005244806.1:p.Ala649= | |
| XM_006710635.2:c.1947C>T | XP_006710698.1:p.Ala649= | |
| XM_011541429.1:c.1947C>T | XP_011539731.1:p.Ala649= | |
| XM_011541430.1:c.1074C>T | XP_011539732.1:p.Ala358= | |
| XM_011541431.1:c.213C>T | XP_011539733.1:p.Ala71= | |
| XR_946650.1:n.2014C>T | ||
| NM_001364727.1:c.1632C>T | NP_001351656.1:p.Ala544= | |
| XM_005244749.3:c.1947C>T | XP_005244806.1:p.Ala649= | |
| XM_011541429.2:c.1947C>T | XP_011539731.1:p.Ala649= | |
| XR_946650.2:n.2018C>T | ||
| NM_001305275.2:c.1947C>T | NP_001292204.1:p.Ala649= | |
| NM_198576.4:c.1947C>T MANE Select | NP_940978.2:p.Ala649= | |
| NM_001364727.2:c.1632C>T | NP_001351656.1:p.Ala544= |