Linked Data
ClinVar Variation Id:
1629644
ClinVar RCV Id:
RCV002125557
dbSNP Id:
rs2153994718
MyVariant Identifiers:
chr11:g.68527106C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68759638C>T , CM000673.2:g.68759638C>T | GRCh38 |
| NC_000011.9:g.68527106C>T , CM000673.1:g.68527106C>T | GRCh37 |
| NC_000011.8:g.68283682C>T | NCBI36 |
| NG_011801.1:g.87294G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265641.10:c.2166G>A MANE Select | ENSP00000265641.4:p.Val722= | |
| ENST00000265641.9:c.2166G>A | ENSP00000265641.4:p.Val722= | |
| ENST00000376618.6:c.2166G>A | ENSP00000365803.2:p.Val722= | |
| ENST00000539743.5:c.2166G>A | ENSP00000446108.1:p.Val722= | |
| ENST00000540367.5:c.2166G>A | ENSP00000439084.1:p.Val722= | |
| NM_001031847.2:c.2166G>A | NP_001027017.1:p.Val722= | |
| NM_001876.3:c.2166G>A | NP_001867.2:p.Val722= | |
| XM_005273762.1:c.2262G>A | XP_005273819.1:p.Val754= | |
| XM_005273763.1:c.2262G>A | XP_005273820.1:p.Val754= | |
| XM_005273762.3:c.2262G>A | XP_005273819.1:p.Val754= | |
| XM_017017220.1:c.2166G>A | XP_016872709.1:p.Val722= | |
| NM_001876.4:c.2166G>A MANE Select | NP_001867.2:p.Val722= | |
| NM_001031847.3:c.2166G>A | NP_001027017.1:p.Val722= |