Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21687172A>G , CM000669.2:g.21687172A>G | GRCh38 |
| NC_000007.13:g.21726790A>G , CM000669.1:g.21726790A>G | GRCh37 |
| NC_000007.12:g.21693315A>G | NCBI36 |
| NG_012886.2:g.148958A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.5695A>G MANE Select | NP_001264044.1:p.Lys1899Glu |
| ENST00000409508.8:c.5695A>G MANE Select | ENSP00000475939.1:p.Lys1899Glu |
| NM_001277115.1:c.5695A>G | NP_001264044.1:p.Lys1899Glu |
| ENST00000328843.10:c.5716A>G | ENSP00000330671.7:p.Lys1906Glu |
| ENST00000409508.7:c.5695A>G | ENSP00000475939.1:p.Lys1899Glu |
| ENST00000620169.4:c.5716A>G | ENSP00000481693.1:p.Lys1906Glu |