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