Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1212353C>T , CM000667.2:g.1212353C>T | GRCh38 |
| NC_000005.9:g.1212468C>T , CM000667.1:g.1212468C>T | GRCh37 |
| NC_000005.8:g.1265468C>T | NCBI36 |
| NG_008282.1:g.15759C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001003841.3:c.532C>T MANE Select | NP_001003841.1:p.Arg178Ter |
| ENST00000304460.11:c.532C>T MANE Select | ENSP00000305302.10:p.Arg178Ter |
| NM_001003841.2:c.532C>T | NP_001003841.1:p.Arg178Ter |
| ENST00000304460.10:c.532C>T | ENSP00000305302.10:p.Arg178Ter |
| ENST00000515652.5:c.440C>T | ENSP00000425701.1:p.Pro147Leu |