Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12789744A= , CM000686.2:g.12789744A= | GRCh38 |
| NC_000024.9:g.14901677A= , CM000686.1:g.14901677A= | GRCh37 |
| NC_000024.8:g.13411071A= | NCBI36 |
| NG_008311.1:g.93518A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651177.1:c.3562-663A= | ENSP00000498372.1:n.3562-663A= | |
| ENST00000338981.7:c.3562-663A= MANE Select | ENSP00000342812.3:n.3562-663A= | |
| ENST00000426564.6:n.3574-663A= | ||
| NM_004654.3:c.3562-663A= | NP_004645.2:n.3562-663A= | |
| XM_011531469.1:c.3562-663A= | XP_011529771.1:n.3562-663A= | |
| XM_011531470.1:c.3328-663A= | XP_011529772.1:n.3328-663A= | |
| XM_017030078.2:c.3577-663A= | XP_016885567.1:n.3577-663A= | |
| NM_004654.4:c.3562-663A= MANE Select | NP_004645.2:n.3562-663A= |