Linked Data
ClinVar Variation Id:
629875
dbSNP Id:
rs781448650
ExAC:
2:215617234 A / G
gnomAD v2:
2-215617234-A-G
gnomAD v3:
2-214752510-A-G
gnomAD v4:
2-214752510-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214752510A>G , CM000664.2:g.214752510A>G | GRCh38 |
| NC_000002.11:g.215617234A>G , CM000664.1:g.215617234A>G | GRCh37 |
| NC_000002.10:g.215325479A>G | NCBI36 |
| NG_012047.2:g.62195T>C | |
| NG_012047.3:g.62202T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.1614T>C MANE Select | ENSP00000260947.4:p.Ser538= | |
| ENST00000421162.2:c.261T>C | ENSP00000392245.2:p.Ser87= | |
| ENST00000613192.2:c.159-22002T>C | ENSP00000483275.2:n.159-22002T>C | |
| ENST00000613374.5:c.204T>C | ENSP00000484464.1:p.Ser68= | |
| ENST00000613706.5:c.1206T>C | ENSP00000484976.2:p.Ser402= | |
| ENST00000617164.5:c.1557T>C | ENSP00000480470.1:p.Ser519= | |
| ENST00000619009.5:c.365-22002T>C | ENSP00000482293.1:n.365-22002T>C | |
| ENST00000650978.1:c.2989T>C | ||
| ENST00000260947.8:c.1614T>C | ENSP00000260947.4:p.Ser538= | |
| ENST00000421162.1:c.261T>C | ENSP00000392245.1:p.Ser87= | |
| ENST00000455743.5:c.*1234T>C | ENSP00000412186.1:n.*1234T>C | |
| ENST00000613192.1:c.74-22002T>C | ENSP00000483275.1:n.74-22002T>C | |
| ENST00000613374.4:c.204T>C | ENSP00000484464.1:p.Ser68= | |
| ENST00000613706.4:c.261T>C | ENSP00000484976.1:p.Ser87= | |
| ENST00000617164.4:c.1557T>C | ENSP00000480470.1:p.Ser519= | |
| ENST00000619009.4:c.365-22002T>C | ENSP00000482293.1:n.365-22002T>C | |
| ENST00000620057.4:c.*280T>C | ENSP00000481988.1:n.*280T>C | |
| NM_000465.3:c.1614T>C | NP_000456.2:p.Ser538= | |
| NM_001282543.1:c.1557T>C | NP_001269472.1:p.Ser519= | |
| NM_001282545.1:c.261T>C | NP_001269474.1:p.Ser87= | |
| NM_001282548.1:c.204T>C | NP_001269477.1:p.Ser68= | |
| NM_001282549.1:c.365-22002T>C | NP_001269478.1:n.365-22002T>C | |
| NR_104212.1:n.1607T>C | ||
| NR_104215.1:n.1550T>C | ||
| NR_104216.1:n.806T>C | ||
| XM_011511567.1:c.1560T>C | XP_011509869.1:p.Ser520= | |
| XM_011511568.1:c.1614T>C | XP_011509870.1:p.Ser538= | |
| XM_017004613.1:c.1713T>C | XP_016860102.1:p.Ser571= | |
| XM_017004614.1:c.1713T>C | XP_016860103.1:p.Ser571= | |
| XR_002959322.1:n.1804T>C | ||
| NM_000465.4:c.1614T>C MANE Select | NP_000456.2:p.Ser538= | |
| NM_001282543.2:c.1557T>C | NP_001269472.1:p.Ser519= | |
| NM_001282545.2:c.261T>C | NP_001269474.1:p.Ser87= | |
| NM_001282548.2:c.204T>C | NP_001269477.1:p.Ser68= | |
| NM_001282549.2:c.365-22002T>C | NP_001269478.1:n.365-22002T>C | |
| NR_104212.2:n.1579T>C | ||
| NR_104215.2:n.1522T>C | ||
| NR_104216.2:n.778T>C |