Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6112224T= , CM000663.2:g.6112224T= | GRCh38 |
| NC_000001.10:g.6172284T= , CM000663.1:g.6172284T= | GRCh37 |
| NC_000001.9:g.6094871T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262450.8:c.5056A= MANE Select | ENSP00000262450.3:p.Lys1686= | |
| ENST00000262450.7:c.5056A= | ENSP00000262450.3:p.Lys1686= | |
| ENST00000377999.5:c.1959A= | ENSP00000367238.2:n.1959A= | |
| ENST00000462991.5:c.3309A= | ||
| ENST00000496404.1:c.3774A= | ENSP00000433676.1:n.3774A= | |
| NM_015557.2:c.5056A= | NP_056372.1:p.Lys1686= | |
| NM_015557.3:c.5056A= MANE Select | NP_056372.1:p.Lys1686= |