Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39504223G>A , CM000681.2:g.39504223G>A | GRCh38 |
| NC_000019.9:g.39994863G>A , CM000681.1:g.39994863G>A | GRCh37 |
| NC_000019.8:g.44686703G>A | NCBI36 |
| NG_008256.1:g.10307G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356433.10:c.805G>A MANE Select | ENSP00000348810.4:p.Gly269Arg | |
| ENST00000205143.4:c.805G>A | ENSP00000205143.3:p.Gly269Arg | |
| ENST00000356433.9:c.805G>A | ENSP00000348810.4:p.Gly269Arg | |
| ENST00000596614.5:c.410-2816G>A | ENSP00000471688.1:n.410-2816G>A | |
| ENST00000600437.1:n.885G>A | ||
| NM_016941.3:c.805G>A | NP_058637.1:p.Gly269Arg | |
| NM_203486.2:c.805G>A | NP_982353.1:p.Gly269Arg | |
| NM_016941.4:c.805G>A | NP_058637.1:p.Gly269Arg | |
| NM_203486.3:c.805G>A MANE Select | NP_982353.1:p.Gly269Arg |