Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23867924G>C , CM000663.2:g.23867924G>C | GRCh38 |
| NC_000001.10:g.24194414G>C , CM000663.1:g.24194414G>C | GRCh37 |
| NC_000001.9:g.24067001G>C | NCBI36 |
| NG_013346.1:g.5446C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.363C>G MANE Select | ENSP00000363603.3:p.Ala121= | |
| ENST00000374479.3:c.363C>G | ENSP00000363603.3:p.Ala121= | |
| NM_000147.4:c.363C>G | NP_000138.2:p.Ala121= | |
| XM_005245821.1:c.-187C>G | XP_005245878.1:n.-187C>G | |
| XM_005245821.3:c.-187C>G | XP_005245878.1:n.-187C>G | |
| NM_000147.5:c.363C>G MANE Select | NP_000138.2:p.Ala121= | |
| NR_174379.1:n.367C>G | ||
| NR_174380.1:n.367C>G | ||
| NR_174381.1:n.367C>G | ||
| NR_174382.1:n.367C>G |