Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.111079821A= , CM000672.2:g.111079821A= | GRCh38 |
| NC_000010.10:g.112839579A= , CM000672.1:g.112839579A= | GRCh37 |
| NC_000010.9:g.112829569A= | NCBI36 |
| NG_012020.1:g.7790A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000681.4:c.*427A= MANE Select | NP_000672.3:n.*427A= |
| ENST00000280155.4:c.*427A= MANE Select | ENSP00000280155.2:n.*427A= |
| NM_000681.3:c.*427A= | NP_000672.3:n.*427A= |
| ENST00000280155.3:c.*427A= | ENSP00000280155.2:n.*427A= |