Linked Data
ClinVar Variation Id:
1903567
ClinVar RCV Id:
RCV002586447
dbSNP Id:
rs769758642
ExAC:
3:69168521 C / T
gnomAD v2:
3-69168521-C-T
gnomAD v4:
3-69119370-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.69119370C>T , CM000665.2:g.69119370C>T | GRCh38 |
| NC_000003.11:g.69168521C>T , CM000665.1:g.69168521C>T | GRCh37 |
| NC_000003.10:g.69251211C>T | NCBI36 |
| NG_041828.1:g.8226G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420581.7:c.985G>A MANE Select | ENSP00000414670.3:p.Ala329Thr | |
| ENST00000420581.6:c.985G>A | ENSP00000414670.2:p.Ala329Thr | |
| ENST00000475434.1:c.985G>A | ENSP00000418645.1:p.Ala329Thr | |
| ENST00000489031.5:c.985G>A | ENSP00000417210.1:p.Ala329Thr | |
| NM_001304418.1:c.985G>A | NP_001291347.1:p.Ala329Thr | |
| NM_198271.4:c.985G>A | NP_938012.2:p.Ala329Thr | |
| NM_001304418.3:c.985G>A | NP_001291347.1:p.Ala329Thr | |
| NM_198271.5:c.985G>A MANE Select | NP_938012.2:p.Ala329Thr |