Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6016226G>A , CM000674.2:g.6016226G>A | GRCh38 |
| NC_000012.11:g.6125392G>A , CM000674.1:g.6125392G>A | GRCh37 |
| NC_000012.10:g.5995653G>A | NCBI36 |
| NG_009072.1:g.113445C>T | |
| NG_009072.2:g.113445C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.5318C>T MANE Select | ENSP00000261405.5:p.Ala1773Val | |
| ENST00000261405.9:c.5318C>T | ENSP00000261405.5:p.Ala1773Val | |
| ENST00000538635.5:n.421-22292C>T | ||
| NM_000552.3:c.5318C>T | NP_000543.2:p.Ala1773Val | |
| NM_000552.4:c.5318C>T | NP_000543.2:p.Ala1773Val | |
| NM_000552.5:c.5318C>T MANE Select | NP_000543.3:p.Ala1773Val |