Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154576404G= , CM000663.2:g.154576404G= | GRCh38 |
| NC_000001.10:g.154548880G= , CM000663.1:g.154548880G= | GRCh37 |
| NC_000001.9:g.152815504G= | NCBI36 |
| NG_008027.1:g.13624G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.*472G= MANE Select | ENSP00000357461.3:n.*472G= | |
| ENST00000636034.1:c.1506-244G= | ENSP00000489703.1:n.1506-244G= | |
| ENST00000637900.1:c.*472G= | ENSP00000490474.1:n.*472G= | |
| ENST00000368476.3:c.*472G= | ENSP00000357461.3:n.*472G= | |
| NM_000748.2:c.*472G= | NP_000739.1:n.*472G= | |
| XM_017000180.2:c.*472G= | XP_016855669.1:n.*472G= | |
| XR_001736952.2:n.2233G= | ||
| NM_000748.3:c.*472G= MANE Select | NP_000739.1:n.*472G= |