Linked Data
ClinVar Variation Id:
430559
ClinVar RCV Id:
RCV000494123
dbSNP Id:
rs369511505
gnomAD v3:
17-14077002-C-T
gnomAD v4:
17-14077002-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.14077002C>T , CM000679.2:g.14077002C>T | GRCh38 |
| NC_000017.10:g.13980319C>T , CM000679.1:g.13980319C>T | GRCh37 |
| NC_000017.9:g.13921044C>T | NCBI36 |
| NG_008034.1:g.12601C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261643.8:c.445C>T MANE Select | ENSP00000261643.3:p.Gln149Ter | |
| ENST00000664217.1:c.445C>T | ENSP00000499396.1:p.Gln149Ter | |
| ENST00000670279.1:c.445C>T | ENSP00000499450.1:p.Gln149Ter | |
| ENST00000261643.7:c.445C>T | ENSP00000261643.3:p.Gln149Ter | |
| ENST00000429152.6:c.445C>T | ENSP00000397750.2:p.Gln149Ter | |
| ENST00000580561.1:c.177+2546C>T | ENSP00000462190.1:n.177+2546C>T | |
| ENST00000581931.5:c.445C>T | ENSP00000462512.1:p.Gln149Ter | |
| NM_001303.3:c.445C>T | NP_001294.2:p.Gln149Ter | |
| XM_005256458.1:c.445C>T | XP_005256515.1:p.Gln149Ter | |
| XM_011523657.1:c.445C>T | XP_011521959.1:p.Gln149Ter | |
| XM_011523658.1:c.-7C>T | XP_011521960.1:n.-7C>T | |
| XR_933974.1:n.548C>T | ||
| XR_933975.1:n.548C>T | ||
| NM_001303.4:c.445C>T MANE Select | NP_001294.2:p.Gln149Ter |