Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46132243G>A , CM000683.2:g.46132243G>A | GRCh38 |
| NC_000021.8:g.47552157G>A , CM000683.1:g.47552157G>A | GRCh37 |
| NC_000021.7:g.46376585G>A | NCBI36 |
| NG_008675.1:g.39125G>A , LRG_476:g.39125G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001849.4:c.2751G>A MANE Select | NP_001840.3:p.Val917= |
| ENST00000300527.9:c.2751G>A MANE Select | ENSP00000300527.4:p.Val917= |
| NM_001849.3:c.2751G>A , LRG_476t1:c.2751G>A | NP_001840.3:p.Val917= |
| ENST00000300527.8:c.2751G>A | ENSP00000300527.4:p.Val917= |
| XM_011529451.1:c.2751G>A | XP_011527753.1:p.Val917= |
| XM_011529452.1:c.2751G>A | XP_011527754.1:p.Val917= |
| XR_937438.1:n.2828G>A | |
| XR_937438.2:n.2835G>A |