Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.20589208A= , CM000663.2:g.20589208A= | GRCh38 |
| NC_000001.10:g.20915701A= , CM000663.1:g.20915701A= | GRCh37 |
| NC_000001.9:g.20788288A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001785.3:c.79A= MANE Select | NP_001776.1:p.Lys27= |
| ENST00000375071.4:c.79A= MANE Select | ENSP00000364212.3:p.Lys27= |
| NM_001785.2:c.79A= | NP_001776.1:p.Lys27= |
| ENST00000375071.3:c.79A= | ENSP00000364212.3:p.Lys27= |
| ENST00000461985.1:n.123A= |