Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29073002T= , CM000664.2:g.29073002T= | GRCh38 |
| NC_000002.11:g.29295868T= , CM000664.1:g.29295868T= | GRCh37 |
| NC_000002.10:g.29149372T= | NCBI36 |
| NG_021427.1:g.6260A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.1260A= MANE Select | ENSP00000332809.4:p.Ala420= | |
| ENST00000331664.5:c.1260A= | ENSP00000332809.4:p.Ala420= | |
| NM_001029883.2:c.1260A= | NP_001025054.1:p.Ala420= | |
| XM_011532826.1:c.1260A= | XP_011531128.1:p.Ala420= | |
| XR_939901.1:n.185+3835T= | ||
| XR_939902.1:n.173+3847T= | ||
| NM_001029883.3:c.1260A= MANE Select | NP_001025054.1:p.Ala420= |