Linked Data
dbSNP Id:
rs1050328
ExAC:
6:31238155 G / A
gnomAD v2:
6-31238155-G-A
gnomAD v3:
6-31270378-G-A
gnomAD v4:
6-31270378-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270378G>A , CM000668.2:g.31270378G>A | GRCh38 |
| NC_000006.11:g.31238155G>A , CM000668.1:g.31238155G>A | GRCh37 |
| NC_000006.10:g.31346134G>A | NCBI36 |
| NG_029422.2:g.6754C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.727C>T MANE Select | ENSP00000365402.5:p.Arg243Trp | |
| ENST00000376228.9:c.727C>T | ENSP00000365402.5:p.Arg243Trp | |
| ENST00000376237.8:c.*314C>T | ENSP00000365412.4:n.*314C>T | |
| ENST00000383329.7:c.727C>T | ENSP00000372819.3:p.Arg243Trp | |
| ENST00000415537.1:c.665-47C>T | ||
| ENST00000470363.5:n.45C>T | ||
| ENST00000487245.5:n.1086C>T | ||
| ENST00000495835.1:n.916C>T | ||
| NM_002117.5:c.727C>T | NP_002108.4:p.Arg243Trp | |
| NM_002117.6:c.727C>T MANE Select | NP_002108.4:p.Arg243Trp |