Linked Data
ClinVar Variation Id:
259442
dbSNP Id:
rs1050931
ExAC:
15:55497691 G / A
gnomAD v2:
15-55497691-G-A
gnomAD v3:
15-55205493-G-A
gnomAD v4:
15-55205493-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.55205493G>A , CM000677.2:g.55205493G>A | GRCh38 |
| NC_000015.9:g.55497691G>A , CM000677.1:g.55497691G>A | GRCh37 |
| NC_000015.8:g.53284983G>A | NCBI36 |
| NG_009103.1:g.89311C>T , LRG_96:g.89311C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000697641.1:n.2716C>T | ||
| ENST00000697642.1:c.*14C>T | ENSP00000513368.1:n.*14C>T | |
| ENST00000697643.1:c.*14C>T | ENSP00000513369.1:n.*14C>T | |
| ENST00000697644.1:n.2848C>T | ||
| ENST00000336787.6:c.*14C>T MANE Select | ENSP00000337761.1:n.*14C>T | |
| ENST00000336787.5:c.*14C>T | ENSP00000337761.1:n.*14C>T | |
| ENST00000396307.6:c.*14C>T | ENSP00000379601.2:n.*14C>T | |
| ENST00000564609.5:c.*14C>T | ENSP00000455012.1:n.*14C>T | |
| ENST00000569493.5:c.*14C>T | ENSP00000456059.1:n.*14C>T | |
| NM_004580.4:c.*14C>T | NP_004571.2:n.*14C>T | |
| NM_183234.2:c.*14C>T | NP_899057.1:n.*14C>T | |
| NM_183235.2:c.*14C>T | NP_899058.1:n.*14C>T | |
| NM_183236.2:c.*14C>T | NP_899059.1:n.*14C>T | |
| XM_005254576.3:c.*14C>T | XP_005254633.1:n.*14C>T | |
| XM_011521852.1:c.*14C>T | XP_011520154.1:n.*14C>T | |
| XM_011521853.1:c.*14C>T | XP_011520155.1:n.*14C>T | |
| XM_011521854.1:c.*14C>T | XP_011520156.1:n.*14C>T | |
| XM_011521855.1:c.*14C>T | XP_011520157.1:n.*14C>T | |
| XM_011521856.1:c.*14C>T | XP_011520158.1:n.*14C>T | |
| XM_005254576.5:c.*14C>T | XP_005254633.1:n.*14C>T | |
| XM_011521855.3:c.*14C>T | XP_011520157.1:n.*14C>T | |
| XM_011521856.2:c.*14C>T | XP_011520158.1:n.*14C>T | |
| XM_024450009.1:c.*14C>T | XP_024305777.1:n.*14C>T | |
| NM_183235.3:c.*14C>T MANE Select | NP_899058.1:n.*14C>T | |
| NM_004580.5:c.*14C>T | NP_004571.2:n.*14C>T | |
| NM_183236.3:c.*14C>T | NP_899059.1:n.*14C>T |