Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68685000C>T , CM000673.2:g.68685000C>T | GRCh38 |
| NC_000011.9:g.68452468C>T , CM000673.1:g.68452468C>T | GRCh37 |
| NC_000011.8:g.68209044C>T | NCBI36 |
| NG_052785.1:g.5526C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015973.5:c.77C>T MANE Select | NP_057057.2:p.Ser26Leu |
| ENST00000265643.4:c.77C>T MANE Select | ENSP00000265643.3:p.Ser26Leu |
| NM_015973.3:c.77C>T | NP_057057.2:p.Ser26Leu |
| NM_015973.4:c.77C>T | NP_057057.2:p.Ser26Leu |
| ENST00000265643.3:c.77C>T | ENSP00000265643.3:p.Ser26Leu |
| XR_001748281.1:n.230+2841G>A |