Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12778082T= , CM000686.2:g.12778082T= | GRCh38 |
| NC_000024.9:g.14890016T= , CM000686.1:g.14890016T= | GRCh37 |
| NC_000024.8:g.13399410T= | NCBI36 |
| NG_008311.1:g.81857T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.2703T= | ENSP00000498372.1:p.Asp901= | |
| ENST00000338981.7:c.2703T= MANE Select | ENSP00000342812.3:p.Asp901= | |
| ENST00000426564.6:n.2715T= | ||
| NM_004654.3:c.2703T= | NP_004645.2:p.Asp901= | |
| XM_011531469.1:c.2703T= | XP_011529771.1:p.Asp901= | |
| XM_011531470.1:c.2469T= | XP_011529772.1:p.Asp823= | |
| XM_017030078.2:c.2718T= | XP_016885567.1:p.Asp906= | |
| NM_004654.4:c.2703T= MANE Select | NP_004645.2:p.Asp901= |