Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20888242A= , CM000684.2:g.20888242A= | GRCh38 |
| NC_000022.10:g.21242530A= , CM000684.1:g.21242530A= | GRCh37 |
| NC_000022.9:g.19572530A= | NCBI36 |
| NG_012152.1:g.34239A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215730.12:c.*406A= MANE Select | ENSP00000215730.6:n.*406A= | |
| ENST00000215730.11:c.*406A= | ENSP00000215730.6:n.*406A= | |
| NM_004782.3:c.*406A= | NP_004773.1:n.*406A= | |
| NM_004782.4:c.*406A= MANE Select | NP_004773.1:n.*406A= |