Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154965993C>A , CM000685.2:g.154965993C>A | GRCh38 |
| NC_000023.10:g.154194268C>A , CM000685.1:g.154194268C>A | GRCh37 |
| NC_000023.9:g.153847462C>A | NCBI36 |
| NG_011403.1:g.61731G>T | |
| NG_011403.2:g.61731G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.1420G>T MANE Select | NP_000123.1:p.Gly474Trp |
| ENST00000360256.9:c.1420G>T MANE Select | ENSP00000353393.4:p.Gly474Trp |
| NM_000132.3:c.1420G>T | NP_000123.1:p.Gly474Trp |
| ENST00000360256.8:c.1420G>T | ENSP00000353393.4:p.Gly474Trp |
| ENST00000483822.2:n.240G>T | |
| ENST00000647125.1:c.*1296G>T | ENSP00000496062.1:n.*1296G>T |
| XM_011531126.1:c.1315G>T | XP_011529428.1:p.Gly439Trp |