Linked Data
ClinVar Variation Id:
1315034
ClinVar RCV Id:
RCV001773228
dbSNP Id:
rs1198645332
gnomAD v2:
1-17322948-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16996453G>T , CM000663.2:g.16996453G>T | GRCh38 |
| NC_000001.10:g.17322948G>T , CM000663.1:g.17322948G>T | GRCh37 |
| NC_000001.9:g.17195535G>T | NCBI36 |
| NG_009054.1:g.20476C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326735.13:c.1239C>A MANE Select | ENSP00000327214.8:p.His413Gln | |
| ENST00000326735.12:c.1239C>A | ENSP00000327214.8:p.His413Gln | |
| ENST00000341676.9:c.1224C>A | ENSP00000341115.5:p.His408Gln | |
| ENST00000452699.5:c.1224C>A | ENSP00000413307.1:p.His408Gln | |
| ENST00000463860.5:n.847C>A | ||
| ENST00000502860.1:n.335-153C>A | ||
| ENST00000506174.5:c.381C>A | ENSP00000424393.1:p.His127Gln | |
| ENST00000509392.1:n.242C>A | ||
| ENST00000617114.4:c.335-153C>A | ENSP00000478781.1:n.335-153C>A | |
| NM_001141973.2:c.1224C>A | NP_001135445.1:p.His408Gln | |
| NM_001141974.2:c.1224C>A | NP_001135446.1:p.His408Gln | |
| NM_022089.3:c.1239C>A | NP_071372.1:p.His413Gln | |
| XM_005245809.1:c.1239C>A | XP_005245866.1:p.His413Gln | |
| XM_005245810.1:c.1236C>A | XP_005245867.1:p.His412Gln | |
| XM_005245811.1:c.1224C>A | XP_005245868.1:p.His408Gln | |
| XM_005245812.1:c.1212C>A | XP_005245869.1:p.His404Gln | |
| XM_005245813.1:c.1239C>A | XP_005245870.1:p.His413Gln | |
| XM_005245815.1:c.1239C>A | XP_005245872.1:p.His413Gln | |
| XM_006710512.1:c.1221C>A | XP_006710575.1:p.His407Gln | |
| XM_006710513.1:c.1197C>A | XP_006710576.1:p.His399Gln | |
| XM_011541128.1:c.1239C>A | XP_011539430.1:p.His413Gln | |
| XM_011541129.1:c.1239C>A | XP_011539431.1:p.His413Gln | |
| XM_017000844.1:c.1239C>A | XP_016856333.1:p.His413Gln | |
| XM_017000845.1:c.1221C>A | XP_016856334.1:p.His407Gln | |
| XM_017000846.1:c.1197C>A | XP_016856335.1:p.His399Gln | |
| XM_017000847.1:c.1209C>A | XP_016856336.1:p.His403Gln | |
| XM_017000848.1:c.1239C>A | XP_016856337.1:p.His413Gln | |
| XM_017000849.1:c.1224C>A | XP_016856338.1:p.His408Gln | |
| XM_017000850.1:c.1239C>A | XP_016856339.1:p.His413Gln | |
| NM_022089.4:c.1239C>A MANE Select | NP_071372.1:p.His413Gln | |
| NM_001141973.3:c.1224C>A | NP_001135445.1:p.His408Gln | |
| NM_001141974.3:c.1224C>A | NP_001135446.1:p.His408Gln |