Linked Data
ClinVar Variation Id:
2845520
ClinVar RCV Id:
RCV003608225
gnomAD v4:
2-214781322-G-C
MyVariant Identifiers:
chr2:g.215646046G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214781322G>C , CM000664.2:g.214781322G>C | GRCh38 |
| NC_000002.11:g.215646046G>C , CM000664.1:g.215646046G>C | GRCh37 |
| NC_000002.10:g.215354291G>C | NCBI36 |
| NG_012047.2:g.33383C>G | |
| NG_012047.3:g.33390C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260947.9:c.552C>G MANE Select | ENSP00000260947.4:p.Ser184= | |
| ENST00000421162.2:c.215+15739C>G | ENSP00000392245.2:n.215+15739C>G | |
| ENST00000613192.2:c.158+28090C>G | ENSP00000483275.2:n.158+28090C>G | |
| ENST00000613374.5:c.158+28090C>G | ENSP00000484464.1:n.158+28090C>G | |
| ENST00000613706.5:c.552C>G | ENSP00000484976.2:p.Ser184= | |
| ENST00000617164.5:c.495C>G | ENSP00000480470.1:p.Ser165= | |
| ENST00000619009.5:c.364+10975C>G | ENSP00000482293.1:n.364+10975C>G | |
| ENST00000650978.1:c.394C>G | ||
| ENST00000260947.8:c.552C>G | ENSP00000260947.4:p.Ser184= | |
| ENST00000421162.1:c.215+15739C>G | ENSP00000392245.1:n.215+15739C>G | |
| ENST00000455743.5:c.*172C>G | ENSP00000412186.1:n.*172C>G | |
| ENST00000471787.1:n.447C>G | ||
| ENST00000613192.1:c.73+28090C>G | ENSP00000483275.1:n.73+28090C>G | |
| ENST00000613374.4:c.158+28090C>G | ENSP00000484464.1:n.158+28090C>G | |
| ENST00000613706.4:c.215+15739C>G | ENSP00000484976.1:n.215+15739C>G | |
| ENST00000617164.4:c.495C>G | ENSP00000480470.1:p.Ser165= | |
| ENST00000619009.4:c.364+10975C>G | ENSP00000482293.1:n.364+10975C>G | |
| ENST00000620057.4:c.364+10975C>G | ENSP00000481988.1:n.364+10975C>G | |
| NM_000465.3:c.552C>G | NP_000456.2:p.Ser184= | |
| NM_001282543.1:c.495C>G | NP_001269472.1:p.Ser165= | |
| NM_001282545.1:c.215+15739C>G | NP_001269474.1:n.215+15739C>G | |
| NM_001282548.1:c.158+28090C>G | NP_001269477.1:n.158+28090C>G | |
| NM_001282549.1:c.364+10975C>G | NP_001269478.1:n.364+10975C>G | |
| NR_104212.1:n.545C>G | ||
| NR_104215.1:n.488C>G | ||
| NR_104216.1:n.506+10975C>G | ||
| XM_011511567.1:c.498C>G | XP_011509869.1:p.Ser166= | |
| XM_011511568.1:c.552C>G | XP_011509870.1:p.Ser184= | |
| XM_017004613.1:c.651C>G | XP_016860102.1:p.Ser217= | |
| XM_017004614.1:c.651C>G | XP_016860103.1:p.Ser217= | |
| XR_002959322.1:n.742C>G | ||
| NM_000465.4:c.552C>G MANE Select | NP_000456.2:p.Ser184= | |
| NM_001282543.2:c.495C>G | NP_001269472.1:p.Ser165= | |
| NM_001282545.2:c.215+15739C>G | NP_001269474.1:n.215+15739C>G | |
| NM_001282548.2:c.158+28090C>G | NP_001269477.1:n.158+28090C>G | |
| NM_001282549.2:c.364+10975C>G | NP_001269478.1:n.364+10975C>G | |
| NR_104212.2:n.517C>G | ||
| NR_104215.2:n.460C>G | ||
| NR_104216.2:n.478+10975C>G |