Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218882184A= , CM000664.2:g.218882184A= | GRCh38 |
| NC_000002.11:g.219746906A= , CM000664.1:g.219746906A= | GRCh37 |
| NC_000002.10:g.219455150A= | NCBI36 |
| NG_012179.1:g.6652A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.137A= MANE Select | ENSP00000258411.3:p.Asp46= | |
| ENST00000258411.7:c.137A= | ENSP00000258411.3:p.Asp46= | |
| ENST00000458582.1:c.24A= | ||
| NM_025216.2:c.137A= | NP_079492.2:p.Asp46= | |
| XM_011511928.1:c.86A= | XP_011510230.1:p.Asp29= | |
| XM_011511929.1:c.41A= | XP_011510231.1:p.Asp14= | |
| XM_011511930.1:c.137A= | XP_011510232.1:p.Asp46= | |
| XM_011511929.2:c.41A= | XP_011510231.1:p.Asp14= | |
| NM_025216.3:c.137A= MANE Select | NP_079492.2:p.Asp46= |