Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186085652A= , CM000666.2:g.186085652A= | GRCh38 |
| NC_000004.11:g.187006806A= , CM000666.1:g.187006806A= | GRCh37 |
| NC_000004.10:g.187243800A= | NCBI36 |
| NG_007278.1:g.21498A= , LRG_117:g.21498A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003265.3:c.*779A= MANE Select | NP_003256.1:n.*779A= |
| ENST00000296795.8:c.*779A= MANE Select | ENSP00000296795.3:n.*779A= |
| ENST00000296795.7:c.*779A= | ENSP00000296795.2:n.*779A= |
| ENST00000698352.1:c.*3046A= | ENSP00000513675.1:n.*3046A= |
| ENST00000698353.1:n.3369A= | |
| ENST00000698354.1:c.*779A= | ENSP00000513676.1:n.*779A= |