Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29534135A= , CM000679.2:g.29534135A= | GRCh38 |
| NC_000017.10:g.27861153A= , CM000679.1:g.27861153A= | GRCh37 |
| NC_000017.9:g.24885279A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261716.8:c.2379A= MANE Select | ENSP00000261716.3:p.Ala793= | |
| ENST00000261716.7:c.2379A= | ENSP00000261716.3:p.Ala793= | |
| ENST00000536202.1:c.1935A= | ENSP00000438819.1:p.Ala645= | |
| NM_020791.2:c.2379A= | NP_065842.1:p.Ala793= | |
| NM_025142.1:c.1935A= | NP_079418.1:p.Ala645= | |
| XM_011525060.1:c.2379A= | XP_011523362.1:p.Ala793= | |
| XM_011525060.2:c.2379A= | XP_011523362.1:p.Ala793= | |
| NM_020791.4:c.2379A= MANE Select | NP_065842.1:p.Ala793= |