Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94491217A>G , CM000663.2:g.94491217A>G | GRCh38 |
| NC_000001.10:g.94956773A>G , CM000663.1:g.94956773A>G | GRCh37 |
| NC_000001.9:g.94729361A>G | NCBI36 |
| NG_008865.1:g.77841A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.1356A>G MANE Select | ENSP00000359233.4:p.Gly452= | |
| ENST00000647998.2:c.1356A>G | ENSP00000497921.2:p.Gly452= | |
| ENST00000370214.8:c.1356A>G | ENSP00000359233.4:p.Gly452= | |
| ENST00000484213.1:n.2206A>G | ||
| NM_002858.3:c.1356A>G | NP_002849.1:p.Gly452= | |
| XM_005271089.2:c.1263A>G | XP_005271146.1:p.Gly421= | |
| XM_006710802.2:c.1428A>G | XP_006710865.2:p.Gly476= | |
| XM_011541877.1:c.420A>G | XP_011540179.1:p.Gly140= | |
| NM_002858.4:c.1356A>G MANE Select | NP_002849.1:p.Gly452= |