Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.59210674A>G , CM000679.2:g.59210674A>G | GRCh38 |
| NC_000017.10:g.57288035A>G , CM000679.1:g.57288035A>G | GRCh37 |
| NC_000017.9:g.54642817A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300917.10:c.623A>G MANE Select | ENSP00000300917.4:p.His208Arg | |
| ENST00000300917.9:c.623A>G | ENSP00000300917.4:p.His208Arg | |
| ENST00000543872.6:c.623A>G | ENSP00000438748.2:p.His208Arg | |
| ENST00000577660.1:c.136-4131A>G | ENSP00000464167.1:n.136-4131A>G | |
| ENST00000578922.1:c.623A>G | ENSP00000462119.1:p.His208Arg | |
| ENST00000580498.5:n.240+413A>G | ||
| NM_018149.6:c.623A>G | NP_060619.4:p.His208Arg | |
| NM_018149.7:c.623A>G MANE Select | NP_060619.4:p.His208Arg |