Linked Data
ClinVar Variation Id:
498321
ClinVar RCV Id:
RCV000593522
dbSNP Id:
rs1553168739
gnomAD v4:
1-16996455-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16996455G>A , CM000663.2:g.16996455G>A | GRCh38 |
| NC_000001.10:g.17322950G>A , CM000663.1:g.17322950G>A | GRCh37 |
| NC_000001.9:g.17195537G>A | NCBI36 |
| NG_009054.1:g.20474C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326735.13:c.1237C>T MANE Select | ENSP00000327214.8:p.His413Tyr | |
| ENST00000326735.12:c.1237C>T | ENSP00000327214.8:p.His413Tyr | |
| ENST00000341676.9:c.1222C>T | ENSP00000341115.5:p.His408Tyr | |
| ENST00000452699.5:c.1222C>T | ENSP00000413307.1:p.His408Tyr | |
| ENST00000463860.5:n.845C>T | ||
| ENST00000502860.1:n.335-155C>T | ||
| ENST00000506174.5:c.379C>T | ENSP00000424393.1:p.His127Tyr | |
| ENST00000509392.1:n.240C>T | ||
| ENST00000617114.4:c.335-155C>T | ENSP00000478781.1:n.335-155C>T | |
| NM_001141973.2:c.1222C>T | NP_001135445.1:p.His408Tyr | |
| NM_001141974.2:c.1222C>T | NP_001135446.1:p.His408Tyr | |
| NM_022089.3:c.1237C>T | NP_071372.1:p.His413Tyr | |
| XM_005245809.1:c.1237C>T | XP_005245866.1:p.His413Tyr | |
| XM_005245810.1:c.1234C>T | XP_005245867.1:p.His412Tyr | |
| XM_005245811.1:c.1222C>T | XP_005245868.1:p.His408Tyr | |
| XM_005245812.1:c.1210C>T | XP_005245869.1:p.His404Tyr | |
| XM_005245813.1:c.1237C>T | XP_005245870.1:p.His413Tyr | |
| XM_005245815.1:c.1237C>T | XP_005245872.1:p.His413Tyr | |
| XM_006710512.1:c.1219C>T | XP_006710575.1:p.His407Tyr | |
| XM_006710513.1:c.1195C>T | XP_006710576.1:p.His399Tyr | |
| XM_011541128.1:c.1237C>T | XP_011539430.1:p.His413Tyr | |
| XM_011541129.1:c.1237C>T | XP_011539431.1:p.His413Tyr | |
| XM_017000844.1:c.1237C>T | XP_016856333.1:p.His413Tyr | |
| XM_017000845.1:c.1219C>T | XP_016856334.1:p.His407Tyr | |
| XM_017000846.1:c.1195C>T | XP_016856335.1:p.His399Tyr | |
| XM_017000847.1:c.1207C>T | XP_016856336.1:p.His403Tyr | |
| XM_017000848.1:c.1237C>T | XP_016856337.1:p.His413Tyr | |
| XM_017000849.1:c.1222C>T | XP_016856338.1:p.His408Tyr | |
| XM_017000850.1:c.1237C>T | XP_016856339.1:p.His413Tyr | |
| NM_022089.4:c.1237C>T MANE Select | NP_071372.1:p.His413Tyr | |
| NM_001141973.3:c.1222C>T | NP_001135445.1:p.His408Tyr | |
| NM_001141974.3:c.1222C>T | NP_001135446.1:p.His408Tyr |