Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88803887G>A , CM000678.2:g.88803887G>A | GRCh38 |
| NC_000016.9:g.88870295G>A , CM000678.1:g.88870295G>A | GRCh37 |
| NC_000016.8:g.87397796G>A | NCBI36 |
| NG_028266.1:g.5110G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301019.9:c.56G>A MANE Select | ENSP00000301019.4:p.Arg19His | |
| ENST00000301019.8:c.56G>A | ENSP00000301019.4:p.Arg19His | |
| NM_030928.3:c.56G>A | NP_112190.2:p.Arg19His | |
| NM_030928.4:c.56G>A MANE Select | NP_112190.2:p.Arg19His |