Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44251531C>T , CM000679.2:g.44251531C>T | GRCh38 |
| NC_000017.10:g.42328899C>T , CM000679.1:g.42328899C>T | GRCh37 |
| NC_000017.9:g.39684425C>T | NCBI36 |
| NG_007498.1:g.21604G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000342.4:c.2369G>A MANE Select | NP_000333.1:p.Gly790Asp |
| ENST00000262418.12:c.2369G>A MANE Select | ENSP00000262418.6:p.Gly790Asp |
| NM_000342.3:c.2369G>A | NP_000333.1:p.Gly790Asp |
| ENST00000262418.10:c.2369G>A | ENSP00000262418.6:p.Gly790Asp |
| ENST00000399246.3:c.1271G>A | ENSP00000382190.3:p.Gly424Asp |
| XM_005257593.3:c.2174G>A | XP_005257650.1:p.Gly725Asp |
| XM_005257593.5:c.2174G>A | XP_005257650.1:p.Gly725Asp |
| XM_011525129.1:c.2279G>A | XP_011523431.1:p.Gly760Asp |
| XM_011525129.2:c.2279G>A | XP_011523431.1:p.Gly760Asp |