Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21002726A= , CM000664.2:g.21002726A= | GRCh38 |
| NC_000002.11:g.21225598A= , CM000664.1:g.21225598A= | GRCh37 |
| NC_000002.10:g.21079103A= | NCBI36 |
| NG_011793.1:g.46348T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.12696T= MANE Select | ENSP00000233242.1:p.Tyr4232= | |
| ENST00000616098.4:c.12696T= | ENSP00000477990.1:p.Tyr4232= | |
| NM_000384.2:c.12696T= | NP_000375.2:p.Tyr4232= | |
| XM_011532809.1:c.5870-3453T= | XP_011531111.1:n.5870-3453T= | |
| NM_000384.3:c.12696T= MANE Select | NP_000375.3:p.Tyr4232= |