Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232522545G>C , CM000664.2:g.232522545G>C | GRCh38 |
| NC_000002.11:g.233387255G>C , CM000664.1:g.233387255G>C | GRCh37 |
| NC_000002.10:g.233095499G>C | NCBI36 |
| NG_008028.1:g.1334G>C | |
| NG_031969.1:g.7083G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001195129.2:c.477G>C MANE Select | NP_001182058.1:p.Thr159= |
| ENST00000617714.2:c.477G>C MANE Select | ENSP00000479745.1:p.Thr159= |
| NM_001195129.1:c.477G>C | NP_001182058.1:p.Thr159= |
| NM_001369848.1:c.477G>C | NP_001356777.1:p.Thr159= |
| ENST00000449534.6:c.477G>C | ENSP00000473410.1:p.Thr159= |
| ENST00000602410.1:n.45G>C | |
| ENST00000617714.1:c.477G>C | ENSP00000479745.1:p.Thr159= |