Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.86032320C>T , CM000664.2:g.86032320C>T | GRCh38 |
| NC_000002.11:g.86259443C>T , CM000664.1:g.86259443C>T | GRCh37 |
| NC_000002.10:g.86112954C>T | NCBI36 |
| NG_050742.2:g.78836G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015425.6:c.4224G>A MANE Select | NP_056240.2:p.Gly1408= |
| ENST00000263857.11:c.4224G>A MANE Select | ENSP00000263857.6:p.Gly1408= |
| NM_015425.3:c.4224G>A | NP_056240.2:p.Gly1408= |
| NM_015425.5:c.4224G>A | NP_056240.2:p.Gly1408= |
| ENST00000263857.10:c.4224G>A | ENSP00000263857.6:p.Gly1408= |
| ENST00000409681.1:c.4224G>A | ENSP00000386300.1:p.Gly1408= |
| ENST00000492034.1:n.408G>A | |
| ENST00000496892.5:n.283G>A | |
| XM_006711983.2:c.3900G>A | XP_006712046.1:p.Gly1300= |