Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49125803C>T , CM000665.2:g.49125803C>T | GRCh38 |
| NC_000003.11:g.49163236C>T , CM000665.1:g.49163236C>T | GRCh37 |
| NC_000003.10:g.49138240C>T | NCBI36 |
| NG_008094.1:g.12364G>A | |
| NG_054716.1:g.136G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002292.4:c.2432G>A MANE Select | NP_002283.3:p.Arg811His |
| ENST00000305544.9:c.2432G>A MANE Select | ENSP00000307156.4:p.Arg811His |
| NM_002292.3:c.2432G>A | NP_002283.3:p.Arg811His |
| ENST00000305544.8:c.2432G>A | ENSP00000307156.4:p.Arg811His |
| ENST00000418109.5:c.2432G>A | ENSP00000388325.1:p.Arg811His |
| ENST00000477701.1:n.305G>A | |
| ENST00000486298.5:n.425+164G>A | |
| ENST00000493571.1:n.342G>A | |
| XM_005265127.3:c.2432G>A | XP_005265184.1:p.Arg811His |
| XM_005265127.4:c.2432G>A | XP_005265184.1:p.Arg811His |