Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48419757C>G , CM000681.2:g.48419757C>G | GRCh38 |
| NC_000019.9:g.48923014C>G , CM000681.1:g.48923014C>G | GRCh37 |
| NC_000019.8:g.53614826C>G | NCBI36 |
| NG_052829.1:g.29883C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263269.4:c.2034C>G MANE Select | ENSP00000263269.2:p.Ala678= | |
| ENST00000263269.3:c.2034C>G | ENSP00000263269.2:p.Ala678= | |
| NM_000836.2:c.2034C>G | NP_000827.2:p.Ala678= | |
| XM_011526872.1:c.2034C>G | XP_011525174.1:p.Ala678= | |
| NM_000836.4:c.2034C>G MANE Select | NP_000827.2:p.Ala678= |