Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17382046T= , CM000663.2:g.17382046T= | GRCh38 |
| NC_000001.10:g.17708541T= , CM000663.1:g.17708541T= | GRCh37 |
| NC_000001.9:g.17581128T= | NCBI36 |
| NG_032943.1:g.14801T= | |
| NG_032943.2:g.14801T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207421.4:c.633T= MANE Select | NP_997304.3:p.His211= |
| ENST00000619609.1:c.633T= MANE Select | ENSP00000483125.1:p.His211= |