Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29534192G= , CM000679.2:g.29534192G= | GRCh38 |
| NC_000017.10:g.27861210G= , CM000679.1:g.27861210G= | GRCh37 |
| NC_000017.9:g.24885336G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261716.8:c.2436G= MANE Select | ENSP00000261716.3:p.Leu812= | |
| ENST00000261716.7:c.2436G= | ENSP00000261716.3:p.Leu812= | |
| ENST00000536202.1:c.1992G= | ENSP00000438819.1:p.Leu664= | |
| NM_020791.2:c.2436G= | NP_065842.1:p.Leu812= | |
| NM_025142.1:c.1992G= | NP_079418.1:p.Leu664= | |
| XM_011525060.1:c.2436G= | XP_011523362.1:p.Leu812= | |
| XM_011525060.2:c.2436G= | XP_011523362.1:p.Leu812= | |
| NM_020791.4:c.2436G= MANE Select | NP_065842.1:p.Leu812= |