Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.120324989C>A , CM000665.2:g.120324989C>A | GRCh38 |
| NC_000003.11:g.120043836C>A , CM000665.1:g.120043836C>A | GRCh37 |
| NC_000003.10:g.121526526C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295628.4:c.*6211G>T MANE Select | ENSP00000295628.3:n.*6211G>T | |
| ENST00000295628.3:c.*6211G>T | ENSP00000295628.3:n.*6211G>T | |
| NM_001099678.1:c.*6211G>T | NP_001093148.1:n.*6211G>T | |
| NM_001099678.2:c.*6211G>T MANE Select | NP_001093148.1:n.*6211G>T |