Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21007469A= , CM000664.2:g.21007469A= | GRCh38 |
| NC_000002.11:g.21230341A= , CM000664.1:g.21230341A= | GRCh37 |
| NC_000002.10:g.21083846A= | NCBI36 |
| NG_011793.1:g.41605T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.9399T= MANE Select | ENSP00000233242.1:p.Pro3133= | |
| ENST00000616098.4:c.9399T= | ENSP00000477990.1:p.Pro3133= | |
| NM_000384.2:c.9399T= | NP_000375.2:p.Pro3133= | |
| XM_011532809.1:c.5869+3264T= | XP_011531111.1:n.5869+3264T= | |
| NM_000384.3:c.9399T= MANE Select | NP_000375.3:p.Pro3133= |