Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30720221G>A , CM000678.2:g.30720221G>A | GRCh38 |
| NC_000016.9:g.30731542G>A , CM000678.1:g.30731542G>A | GRCh37 |
| NC_000016.8:g.30639043G>A | NCBI36 |
| NG_032135.1:g.26081G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006662.3:c.2877G>A MANE Select | NP_006653.2:p.Glu959= |
| ENST00000262518.9:c.2877G>A MANE Select | ENSP00000262518.4:p.Glu959= |
| NM_006662.2:c.2877G>A | NP_006653.2:p.Glu959= |
| ENST00000262518.8:c.2877G>A | ENSP00000262518.4:p.Glu959= |
| ENST00000380361.7:c.2820G>A | ENSP00000369719.3:p.Glu940= |
| ENST00000395059.6:c.2286G>A | ENSP00000378499.3:p.Glu762= |
| ENST00000411466.7:c.2877G>A | ENSP00000405186.3:p.Glu959= |
| ENST00000483083.3:c.1976G>A | |
| ENST00000706321.1:c.2877G>A | ENSP00000516346.1:p.Glu959= |