Linked Data
ClinVar Variation Id:
902910
dbSNP Id:
rs764846938
ExAC:
3:49162453 C / T
gnomAD v2:
3-49162453-C-T
gnomAD v3:
3-49125020-C-T
gnomAD v4:
3-49125020-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49125020C>T , CM000665.2:g.49125020C>T | GRCh38 |
| NC_000003.11:g.49162453C>T , CM000665.1:g.49162453C>T | GRCh37 |
| NC_000003.10:g.49137457C>T | NCBI36 |
| NG_008094.1:g.13147G>A | |
| NG_054716.1:g.919G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.2870G>A MANE Select | ENSP00000307156.4:p.Arg957Gln | |
| ENST00000305544.8:c.2870G>A | ENSP00000307156.4:p.Arg957Gln | |
| ENST00000418109.5:c.2870G>A | ENSP00000388325.1:p.Arg957Gln | |
| ENST00000462930.5:n.277G>A | ||
| ENST00000464891.5:n.603G>A | ||
| ENST00000483057.1:n.470G>A | ||
| ENST00000486298.5:n.575G>A | ||
| ENST00000542580.1:n.185G>A | ||
| NM_002292.3:c.2870G>A | NP_002283.3:p.Arg957Gln | |
| XM_005265127.3:c.2870G>A | XP_005265184.1:p.Arg957Gln | |
| XM_005265127.4:c.2870G>A | XP_005265184.1:p.Arg957Gln | |
| NM_002292.4:c.2870G>A MANE Select | NP_002283.3:p.Arg957Gln |