Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785540C>T , CM000681.2:g.18785540C>T | GRCh38 |
| NC_000019.9:g.18896350C>T , CM000681.1:g.18896350C>T | GRCh37 |
| NC_000019.8:g.18757350C>T | NCBI36 |
| NG_007070.1:g.10765G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1675G>A MANE Select | ENSP00000222271.2:p.Glu559Lys | |
| ENST00000222271.6:c.1675G>A | ENSP00000222271.2:p.Glu559Lys | |
| ENST00000425807.1:c.1516G>A | ENSP00000403792.1:p.Glu506Lys | |
| ENST00000542601.6:c.1576G>A | ENSP00000439156.2:p.Glu526Lys | |
| NM_000095.2:c.1675G>A | NP_000086.2:p.Glu559Lys | |
| NM_000095.3:c.1675G>A MANE Select | NP_000086.2:p.Glu559Lys |