Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147918680A>T , CM000669.2:g.147918680A>T | GRCh38 |
| NC_000007.13:g.147615772A>T , CM000669.1:g.147615772A>T | GRCh37 |
| NC_000007.12:g.147246705A>T | NCBI36 |
| NG_007092.2:g.1807320A>T | |
| NG_007092.3:g.1807680A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.2255+14959A>T MANE Select | ENSP00000354778.3:n.2255+14959A>T | |
| ENST00000636870.1:n.2117+14959A>T | ||
| ENST00000637825.1:n.1738+14959A>T | ||
| ENST00000361727.7:c.2255+14959A>T | ENSP00000354778.3:n.2255+14959A>T | |
| ENST00000455301.2:n.190+14959A>T | ||
| ENST00000627772.2:n.428+14959A>T | ||
| NM_014141.5:c.2255+14959A>T | NP_054860.1:n.2255+14959A>T | |
| XM_006715919.1:c.743+14959A>T | XP_006715982.1:n.743+14959A>T | |
| NM_014141.6:c.2255+14959A>T MANE Select | NP_054860.1:n.2255+14959A>T |