Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4934365A>C , CM000679.2:g.4934365A>C | GRCh38 |
| NC_000017.10:g.4837660A>C , CM000679.1:g.4837660A>C | GRCh37 |
| NC_000017.9:g.4778401A>C | NCBI36 |
| NG_008767.2:g.7071A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000173.7:c.1761A>C (GP1BA) MANE Select | NP_000164.5:p.Gln587His |
| ENST00000329125.6:c.1761A>C (GP1BA) MANE Select | ENSP00000329380.5:p.Gln587His |
| NM_000173.6:c.1761A>C (GP1BA) | NP_000164.5:p.Gln587His |
| ENST00000329125.5:c.1761A>C (GP1BA) | ENSP00000329380.5:p.Gln587His |
| ENST00000611961.1:c.1683A>C (GP1BA) | ENSP00000484439.1:p.Gln561His |
| ENST00000649830.1:c.-911T>G (CHRNE) | ENSP00000496907.1:n.-911T>G |