Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29232439C>A , CM000664.2:g.29232439C>A | GRCh38 |
| NC_000002.11:g.29455305C>A , CM000664.1:g.29455305C>A | GRCh37 |
| NC_000002.10:g.29308809C>A | NCBI36 |
| NG_009445.1:g.694128G>T , LRG_488:g.694128G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004304.5:c.2497G>T MANE Select | NP_004295.2:p.Gly833Ter |
| ENST00000389048.8:c.2497G>T MANE Select | ENSP00000373700.3:p.Gly833Ter |
| NM_004304.4:c.2497G>T | NP_004295.2:p.Gly833Ter |
| ENST00000389048.7:c.2497G>T | ENSP00000373700.3:p.Gly833Ter |
| ENST00000618119.4:c.1366G>T | ENSP00000482733.1:p.Gly456Ter |
| XR_001738688.2:n.3427G>T |