ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7222807G>T , CM000679.2:g.7222807G>T | GRCh38 |
| NC_000017.10:g.7126126G>T , CM000679.1:g.7126126G>T | GRCh37 |
| NC_000017.9:g.7066850G>T | NCBI36 |
| NG_007975.1:g.7974G>T | |
| NG_008391.2:g.2244C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1019G>T MANE Select | ENSP00000349297.5:p.Gly340Val | |
| ENST00000322910.9:c.*974G>T | ENSP00000325395.5:n.*974G>T | |
| ENST00000350303.9:c.953G>T | ENSP00000344152.5:p.Gly318Val | |
| ENST00000356839.9:c.1019G>T | ENSP00000349297.5:p.Gly340Val | |
| ENST00000543245.6:c.1088G>T | ENSP00000438689.2:p.Gly363Val | |
| ENST00000578824.5:n.168G>T | ||
| ENST00000581378.5:c.737G>T | ||
| ENST00000582379.1:n.403G>T | ||
| ENST00000583858.5:c.48G>T | ||
| NM_000018.3:c.1019G>T | NP_000009.1:p.Gly340Val | |
| NM_001033859.2:c.953G>T | NP_001029031.1:p.Gly318Val | |
| NM_001270447.1:c.1088G>T | NP_001257376.1:p.Gly363Val | |
| NM_001270448.1:c.791G>T | NP_001257377.1:p.Gly264Val | |
| XM_006721516.2:c.1019G>T | XP_006721579.2:p.Gly340Val | |
| XM_011523829.1:c.1019G>T | XP_011522131.1:p.Gly340Val | |
| XM_011523830.1:c.1019G>T | XP_011522132.1:p.Gly340Val | |
| XR_934021.1:n.1126G>T | ||
| XR_934022.1:n.1126G>T | ||
| XR_934023.1:n.1126G>T | ||
| XM_006721516.3:c.1019G>T | XP_006721579.2:p.Gly340Val | |
| XM_011523829.2:c.1019G>T | XP_011522131.1:p.Gly340Val | |
| XM_011523830.2:c.1019G>T | XP_011522132.1:p.Gly340Val | |
| XM_024450741.1:c.1019G>T | XP_024306509.1:p.Gly340Val | |
| XR_934021.2:n.1078G>T | ||
| XR_934022.2:n.1078G>T | ||
| XR_934023.2:n.1078G>T | ||
| NM_000018.4:c.1019G>T MANE Select | NP_000009.1:p.Gly340Val | |
| NM_001033859.3:c.953G>T | NP_001029031.1:p.Gly318Val | |
| NM_001270447.2:c.1088G>T | NP_001257376.1:p.Gly363Val | |
| NM_001270448.2:c.791G>T | NP_001257377.1:p.Gly264Val |