Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147879319C>T , CM000669.2:g.147879319C>T | GRCh38 |
| NC_000007.13:g.147576411C>T , CM000669.1:g.147576411C>T | GRCh37 |
| NC_000007.12:g.147207344C>T | NCBI36 |
| NG_007092.2:g.1767959C>T | |
| NG_007092.3:g.1768319C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014141.6:c.2099-24246C>T MANE Select | NP_054860.1:n.2099-24246C>T |
| ENST00000361727.8:c.2099-24246C>T MANE Select | ENSP00000354778.3:n.2099-24246C>T |
| NM_014141.5:c.2099-24246C>T | NP_054860.1:n.2099-24246C>T |
| ENST00000361727.7:c.2099-24246C>T | ENSP00000354778.3:n.2099-24246C>T |
| ENST00000455301.2:n.34-24246C>T | |
| ENST00000627772.2:n.272-24246C>T | |
| ENST00000636870.1:n.1961-24246C>T | |
| ENST00000637825.1:n.1582-24246C>T | |
| XM_006715919.1:c.587-24246C>T | XP_006715982.1:n.587-24246C>T |