Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.83907067T>C , CM000678.2:g.83907067T>C | GRCh38 |
| NC_000016.9:g.83940672T>C , CM000678.1:g.83940672T>C | GRCh37 |
| NC_000016.8:g.82498173T>C | NCBI36 |
| NG_009079.1:g.12943T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012213.3:c.609T>C MANE Select | NP_036345.2:p.His203= |
| ENST00000262430.6:c.609T>C MANE Select | ENSP00000262430.4:p.His203= |
| NM_012213.2:c.609T>C | NP_036345.2:p.His203= |
| ENST00000262430.5:c.609T>C | ENSP00000262430.4:p.His203= |