Linked Data
ClinVar Variation Id:
142728
dbSNP Id:
rs587782675
gnomAD v3:
2-214809475-C-A
gnomAD v4:
2-214809475-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214809475C>A , CM000664.2:g.214809475C>A | GRCh38 |
| NC_000002.11:g.215674199C>A , CM000664.1:g.215674199C>A | GRCh37 |
| NC_000002.10:g.215382444C>A | NCBI36 |
| NG_012047.2:g.5230G>T | |
| NG_012047.3:g.5237G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.95G>T MANE Select | ENSP00000260947.4:p.Gly32Val | |
| ENST00000421162.2:c.95G>T | ENSP00000392245.2:p.Gly32Val | |
| ENST00000613192.2:c.95G>T | ENSP00000483275.2:p.Gly32Val | |
| ENST00000613374.5:c.95G>T | ENSP00000484464.1:p.Gly32Val | |
| ENST00000613706.5:c.95G>T | ENSP00000484976.2:p.Gly32Val | |
| ENST00000617164.5:c.95G>T | ENSP00000480470.1:p.Gly32Val | |
| ENST00000619009.5:c.95G>T | ENSP00000482293.1:p.Gly32Val | |
| ENST00000260947.8:c.95G>T | ENSP00000260947.4:p.Gly32Val | |
| ENST00000421162.1:c.95G>T | ENSP00000392245.1:p.Gly32Val | |
| ENST00000455743.5:c.95G>T | ENSP00000412186.1:p.Gly32Val | |
| ENST00000471787.1:n.196G>T | ||
| ENST00000479904.1:n.186G>T | ||
| ENST00000613192.1:c.10G>T | ENSP00000483275.1:p.Val4Leu | |
| ENST00000613374.4:c.95G>T | ENSP00000484464.1:p.Gly32Val | |
| ENST00000613706.4:c.95G>T | ENSP00000484976.1:p.Gly32Val | |
| ENST00000617164.4:c.95G>T | ENSP00000480470.1:p.Gly32Val | |
| ENST00000619009.4:c.95G>T | ENSP00000482293.1:p.Gly32Val | |
| ENST00000620057.4:c.95G>T | ENSP00000481988.1:p.Gly32Val | |
| NM_000465.3:c.95G>T | NP_000456.2:p.Gly32Val | |
| NM_001282543.1:c.95G>T | NP_001269472.1:p.Gly32Val | |
| NM_001282545.1:c.95G>T | NP_001269474.1:p.Gly32Val | |
| NM_001282548.1:c.95G>T | NP_001269477.1:p.Gly32Val | |
| NM_001282549.1:c.95G>T | NP_001269478.1:p.Gly32Val | |
| NR_104212.1:n.237G>T | ||
| NR_104215.1:n.237G>T | ||
| NR_104216.1:n.237G>T | ||
| XM_011511568.1:c.95G>T | XP_011509870.1:p.Gly32Val | |
| XM_017004613.1:c.95G>T | XP_016860102.1:p.Gly32Val | |
| XM_017004614.1:c.95G>T | XP_016860103.1:p.Gly32Val | |
| XR_002959322.1:n.186G>T | ||
| NM_000465.4:c.95G>T MANE Select | NP_000456.2:p.Gly32Val | |
| NM_001282543.2:c.95G>T | NP_001269472.1:p.Gly32Val | |
| NM_001282545.2:c.95G>T | NP_001269474.1:p.Gly32Val | |
| NM_001282548.2:c.95G>T | NP_001269477.1:p.Gly32Val | |
| NM_001282549.2:c.95G>T | NP_001269478.1:p.Gly32Val | |
| NR_104212.2:n.209G>T | ||
| NR_104215.2:n.209G>T | ||
| NR_104216.2:n.209G>T |