Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152648904G>A , CM000669.2:g.152648904G>A | GRCh38 |
| NC_000007.13:g.152345989G>A , CM000669.1:g.152345989G>A | GRCh37 |
| NC_000007.12:g.151976922G>A | NCBI36 |
| NG_027988.1:g.32262C>T | |
| NG_027988.2:g.32262C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005431.2:c.581C>T MANE Select | NP_005422.1:p.Thr194Met |
| ENST00000359321.2:c.581C>T MANE Select | ENSP00000352271.1:p.Thr194Met |
| NM_005431.1:c.581C>T | NP_005422.1:p.Thr194Met |
| ENST00000359321.1:c.581C>T | ENSP00000352271.1:p.Thr194Met |
| ENST00000495707.1:n.603C>T | |
| ENST00000698506.1:c.413C>T | ENSP00000513758.1:p.Thr138Met |