Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21001691A= , CM000664.2:g.21001691A= | GRCh38 |
| NC_000002.11:g.21224563A= , CM000664.1:g.21224563A= | GRCh37 |
| NC_000002.10:g.21078068A= | NCBI36 |
| NG_011793.1:g.47383T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.*39T= MANE Select | ENSP00000233242.1:n.*39T= | |
| ENST00000616098.4:c.13729T= | ENSP00000477990.1:n.13729T= | |
| NM_000384.2:c.*39T= | NP_000375.2:n.*39T= | |
| XM_011532809.1:c.5870-2418T= | XP_011531111.1:n.5870-2418T= | |
| NM_000384.3:c.*39T= MANE Select | NP_000375.3:n.*39T= |