Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.7015722C= , CM000680.2:g.7015722C= | GRCh38 |
| NC_000018.9:g.7015721C= , CM000680.1:g.7015721C= | GRCh37 |
| NC_000018.8:g.7005721C= | NCBI36 |
| NG_034251.1:g.107093G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389658.4:c.3126G= MANE Select | ENSP00000374309.3:p.Gln1042= | |
| ENST00000389658.3:c.3126G= | ENSP00000374309.3:p.Gln1042= | |
| ENST00000579014.5:n.4141G= | ||
| NM_005559.3:c.3126G= | NP_005550.2:p.Gln1042= | |
| XM_011525655.1:c.3126G= | XP_011523957.1:p.Gln1042= | |
| XM_011525656.1:c.1554G= | XP_011523958.1:p.Gln518= | |
| XM_011525657.1:c.3126G= | XP_011523959.1:p.Gln1042= | |
| XM_011525655.2:c.3126G= | XP_011523957.1:p.Gln1042= | |
| XM_011525656.2:c.1554G= | XP_011523958.1:p.Gln518= | |
| NM_005559.4:c.3126G= MANE Select | NP_005550.2:p.Gln1042= |