Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15440340C>T , CM000663.2:g.15440340C>T | GRCh38 |
| NC_000001.10:g.15766836C>T , CM000663.1:g.15766836C>T | GRCh37 |
| NC_000001.9:g.15639423C>T | NCBI36 |
| NG_009253.1:g.6899C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007272.3:c.81C>T MANE Select | NP_009203.2:p.Ser27= |
| ENST00000375949.5:c.81C>T MANE Select | ENSP00000365116.4:p.Ser27= |
| NM_007272.2:c.81C>T | NP_009203.2:p.Ser27= |
| ENST00000375943.6:c.40+1836C>T | ENSP00000365110.2:n.40+1836C>T |
| ENST00000375949.4:c.81C>T | ENSP00000365116.4:p.Ser27= |
| ENST00000476813.5:n.52+1836C>T | |
| XM_011540550.1:c.81C>T | XP_011538852.1:p.Ser27= |