Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6112277T= , CM000663.2:g.6112277T= | GRCh38 |
| NC_000001.10:g.6172337T= , CM000663.1:g.6172337T= | GRCh37 |
| NC_000001.9:g.6094924T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262450.8:c.5003A= MANE Select | ENSP00000262450.3:p.Asp1668= | |
| ENST00000262450.7:c.5003A= | ENSP00000262450.3:p.Asp1668= | |
| ENST00000377999.5:c.1906A= | ENSP00000367238.2:n.1906A= | |
| ENST00000462991.5:c.3256A= | ||
| ENST00000496404.1:c.3721A= | ENSP00000433676.1:n.3721A= | |
| NM_015557.2:c.5003A= | NP_056372.1:p.Asp1668= | |
| NM_015557.3:c.5003A= MANE Select | NP_056372.1:p.Asp1668= |