Linked Data
dbSNP Id:
rs1432239546
gnomAD v2:
1-59248162-C-T
gnomAD v3:
1-58782490-C-T
gnomAD v4:
1-58782490-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58782490C>T , CM000663.2:g.58782490C>T | GRCh38 |
| NC_000001.10:g.59248162C>T , CM000663.1:g.59248162C>T | GRCh37 |
| NC_000001.9:g.59020750C>T | NCBI36 |
| NG_047027.1:g.6624G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710273.1:c.647G>A | ENSP00000518166.1:p.Gly216Asp | |
| ENST00000371222.4:c.581G>A MANE Select | ENSP00000360266.2:p.Gly194Asp | |
| ENST00000678696.1:c.581G>A | ENSP00000503132.1:p.Gly194Asp | |
| ENST00000371222.3:c.581G>A | ENSP00000360266.2:p.Gly194Asp | |
| NM_002228.3:c.581G>A | NP_002219.1:p.Gly194Asp | |
| NM_002228.4:c.581G>A MANE Select | NP_002219.1:p.Gly194Asp |