Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24291003G>A , CM000668.2:g.24291003G>A | GRCh38 |
| NC_000006.11:g.24291231G>A , CM000668.1:g.24291231G>A | GRCh37 |
| NC_000006.10:g.24399210G>A | NCBI36 |
| NG_012829.1:g.72050C>T | |
| NG_012829.2:g.97290C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.633C>T MANE Select | ENSP00000367715.3:p.Gly211= | |
| ENST00000378454.7:c.633C>T | ENSP00000367715.3:p.Gly211= | |
| NM_001195610.1:c.633C>T | NP_001182539.1:p.Gly211= | |
| NM_016356.4:c.633C>T | NP_057440.2:p.Gly211= | |
| NM_016356.5:c.633C>T MANE Select | NP_057440.2:p.Gly211= | |
| NM_001195610.2:c.633C>T | NP_001182539.1:p.Gly211= |