Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48858508G>A , CM000665.2:g.48858508G>A | GRCh38 |
| NC_000003.11:g.48895941G>A , CM000665.1:g.48895941G>A | GRCh37 |
| NC_000003.10:g.48870945G>A | NCBI36 |
| NG_008171.1:g.45389C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000387.6:c.842C>T MANE Select | NP_000378.1:p.Ala281Val |
| ENST00000319017.5:c.842C>T MANE Select | ENSP00000326305.4:p.Ala281Val |
| NM_000387.5:c.842C>T | NP_000378.1:p.Ala281Val |
| ENST00000319017.4:c.842C>T | ENSP00000326305.4:p.Ala281Val |
| ENST00000430379.5:c.623C>T | ENSP00000388986.1:p.Ala208Val |
| ENST00000440964.1:c.*672C>T | ENSP00000388563.1:n.*672C>T |
| ENST00000479050.1:n.161C>T | |
| XM_006713327.1:c.536-736C>T | XP_006713390.1:n.536-736C>T |