Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48892057G>A , CM000665.2:g.48892057G>A | GRCh38 |
| NC_000003.11:g.48929490G>A , CM000665.1:g.48929490G>A | GRCh37 |
| NC_000003.10:g.48904494G>A | NCBI36 |
| NG_008171.1:g.11840C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000387.6:c.121C>T MANE Select | NP_000378.1:p.Gln41Ter |
| ENST00000319017.5:c.121C>T MANE Select | ENSP00000326305.4:p.Gln41Ter |
| NM_000387.5:c.121C>T | NP_000378.1:p.Gln41Ter |
| ENST00000319017.4:c.121C>T | ENSP00000326305.4:p.Gln41Ter |
| ENST00000430379.5:c.121C>T | ENSP00000388986.1:p.Gln41Ter |
| ENST00000440964.1:c.182C>T | ENSP00000388563.1:p.Thr61Ile |
| XM_006713327.1:c.121C>T | XP_006713390.1:p.Gln41Ter |