Linked Data
ClinVar Variation Id:
2587274
ClinVar RCV Id:
RCV003350648
dbSNP Id:
rs781020785
gnomAD v4:
12-40309218-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.40309218G>T , CM000674.2:g.40309218G>T | GRCh38 |
| NC_000012.11:g.40703020G>T , CM000674.1:g.40703020G>T | GRCh37 |
| NC_000012.10:g.38989287G>T | NCBI36 |
| NG_011709.1:g.89208G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298910.12:c.4302G>T MANE Select | ENSP00000298910.7:p.Trp1434Cys | |
| ENST00000679360.1:c.*3211G>T | ENSP00000505368.1:n.*3211G>T | |
| ENST00000680790.1:c.4047G>T | ENSP00000505335.1:p.Trp1349Cys | |
| ENST00000298910.11:c.4302G>T | ENSP00000298910.7:p.Trp1434Cys | |
| ENST00000430804.5:c.1598G>T | ||
| ENST00000479187.5:n.983G>T | ||
| NM_198578.3:c.4302G>T | NP_940980.3:p.Trp1434Cys | |
| XM_005268629.2:c.4302G>T | XP_005268686.1:p.Trp1434Cys | |
| XM_011537877.1:c.4302G>T | XP_011536179.1:p.Trp1434Cys | |
| XM_011537878.1:c.4302G>T | XP_011536180.1:p.Trp1434Cys | |
| XM_011537879.1:c.3099G>T | XP_011536181.1:p.Trp1033Cys | |
| XM_011537880.1:c.4302G>T | XP_011536182.1:p.Trp1434Cys | |
| XM_011537881.1:c.4302G>T | XP_011536183.1:p.Trp1434Cys | |
| XM_005268629.4:c.4302G>T | XP_005268686.1:p.Trp1434Cys | |
| XM_011537877.3:c.4302G>T | XP_011536179.1:p.Trp1434Cys | |
| XM_011537881.3:c.4302G>T | XP_011536183.1:p.Trp1434Cys | |
| XM_017018786.2:c.4302G>T | XP_016874275.1:p.Trp1434Cys | |
| XM_017018787.1:c.1218G>T | XP_016874276.1:p.Trp406Cys | |
| XM_017018788.2:c.564G>T | XP_016874277.1:p.Trp188Cys | |
| XM_024448833.1:c.3099G>T | XP_024304601.1:p.Trp1033Cys | |
| XR_001748574.2:n.4544G>T | ||
| NM_198578.4:c.4302G>T MANE Select | NP_940980.4:p.Trp1434Cys |