Linked Data
ClinVar Variation Id:
672309
dbSNP Id:
rs968535447
gnomAD v3:
2-214745089-T-G
gnomAD v4:
2-214745089-T-G
MyVariant Identifiers:
chr2:g.215609813T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214745089T>G , CM000664.2:g.214745089T>G | GRCh38 |
| NC_000002.11:g.215609813T>G , CM000664.1:g.215609813T>G | GRCh37 |
| NC_000002.10:g.215318058T>G | NCBI36 |
| NG_012047.2:g.69616A>C | |
| NG_012047.3:g.69623A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.1881A>C MANE Select | ENSP00000260947.4:p.Gly627= | |
| ENST00000421162.2:c.528A>C | ENSP00000392245.2:p.Gly176= | |
| ENST00000613192.2:c.159-14581A>C | ENSP00000483275.2:n.159-14581A>C | |
| ENST00000613374.5:c.471A>C | ENSP00000484464.1:p.Gly157= | |
| ENST00000613706.5:c.1473A>C | ENSP00000484976.2:p.Gly491= | |
| ENST00000617164.5:c.1824A>C | ENSP00000480470.1:p.Gly608= | |
| ENST00000619009.5:c.365-14581A>C | ENSP00000482293.1:n.365-14581A>C | |
| ENST00000650978.1:c.3256A>C | ||
| ENST00000260947.8:c.1881A>C | ENSP00000260947.4:p.Gly627= | |
| ENST00000421162.1:c.528A>C | ENSP00000392245.1:p.Gly176= | |
| ENST00000455743.5:c.*1501A>C | ENSP00000412186.1:n.*1501A>C | |
| ENST00000613192.1:c.74-14581A>C | ENSP00000483275.1:n.74-14581A>C | |
| ENST00000613374.4:c.471A>C | ENSP00000484464.1:p.Gly157= | |
| ENST00000613706.4:c.528A>C | ENSP00000484976.1:p.Gly176= | |
| ENST00000617164.4:c.1824A>C | ENSP00000480470.1:p.Gly608= | |
| ENST00000619009.4:c.365-14581A>C | ENSP00000482293.1:n.365-14581A>C | |
| ENST00000620057.4:c.*547A>C | ENSP00000481988.1:n.*547A>C | |
| NM_000465.3:c.1881A>C | NP_000456.2:p.Gly627= | |
| NM_001282543.1:c.1824A>C | NP_001269472.1:p.Gly608= | |
| NM_001282545.1:c.528A>C | NP_001269474.1:p.Gly176= | |
| NM_001282548.1:c.471A>C | NP_001269477.1:p.Gly157= | |
| NM_001282549.1:c.365-14581A>C | NP_001269478.1:n.365-14581A>C | |
| NR_104212.1:n.1874A>C | ||
| NR_104215.1:n.1817A>C | ||
| NR_104216.1:n.1073A>C | ||
| XM_011511567.1:c.1827A>C | XP_011509869.1:p.Gly609= | |
| XM_011511568.1:c.1881A>C | XP_011509870.1:p.Gly627= | |
| XM_017004613.1:c.1980A>C | XP_016860102.1:p.Gly660= | |
| XM_017004614.1:c.1980A>C | XP_016860103.1:p.Gly660= | |
| XR_002959322.1:n.2071A>C | ||
| NM_000465.4:c.1881A>C MANE Select | NP_000456.2:p.Gly627= | |
| NM_001282543.2:c.1824A>C | NP_001269472.1:p.Gly608= | |
| NM_001282545.2:c.528A>C | NP_001269474.1:p.Gly176= | |
| NM_001282548.2:c.471A>C | NP_001269477.1:p.Gly157= | |
| NM_001282549.2:c.365-14581A>C | NP_001269478.1:n.365-14581A>C | |
| NR_104212.2:n.1846A>C | ||
| NR_104215.2:n.1789A>C | ||
| NR_104216.2:n.1045A>C |