Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20888212T= , CM000684.2:g.20888212T= | GRCh38 |
| NC_000022.10:g.21242500T= , CM000684.1:g.21242500T= | GRCh37 |
| NC_000022.9:g.19572500T= | NCBI36 |
| NG_012152.1:g.34209T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215730.12:c.*376T= MANE Select | ENSP00000215730.6:n.*376T= | |
| ENST00000215730.11:c.*376T= | ENSP00000215730.6:n.*376T= | |
| NM_004782.3:c.*376T= | NP_004773.1:n.*376T= | |
| NM_004782.4:c.*376T= MANE Select | NP_004773.1:n.*376T= |