Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129822779G>A , CM000671.2:g.129822779G>A | GRCh38 |
| NC_000009.11:g.132585058G>A , CM000671.1:g.132585058G>A | GRCh37 |
| NC_000009.10:g.131624879G>A | NCBI36 |
| NG_008049.1:g.6384C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000113.3:c.246C>T MANE Select | NP_000104.1:p.Ala82= |
| ENST00000351698.5:c.246C>T MANE Select | ENSP00000345719.4:p.Ala82= |
| NM_000113.2:c.246C>T | NP_000104.1:p.Ala82= |
| ENST00000351698.4:c.246C>T | ENSP00000345719.4:p.Ala82= |
| ENST00000473084.1:n.265C>T | |
| ENST00000473604.2:n.356C>T | |
| ENST00000651202.1:c.342C>T | ENSP00000498222.1:p.Ala114= |
| XR_929731.1:n.406C>T | |
| XR_929731.3:n.274C>T |