Linked Data
ClinVar Variation Id:
1613302
ClinVar RCV Id:
RCV002171202
dbSNP Id:
rs1237225997
MyVariant Identifiers:
chr5:g.131924434A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132588742A>G , CM000667.2:g.132588742A>G | GRCh38 |
| NC_000005.9:g.131924434A>G , CM000667.1:g.131924434A>G | GRCh37 |
| NC_000005.8:g.131952333A>G | NCBI36 |
| NG_021151.1:g.36819A>G | |
| NG_021151.2:g.36766A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378823.8:c.1107A>G MANE Select | ENSP00000368100.4:p.Ser369= | |
| ENST00000638452.2:c.810A>G | ENSP00000492349.2:p.Ser270= | |
| ENST00000638504.1:n.793A>G | ||
| ENST00000638568.2:c.810A>G | ENSP00000491158.2:p.Ser270= | |
| ENST00000639899.1:n.1626A>G | ||
| ENST00000640655.2:c.810A>G | ENSP00000491596.2:p.Ser270= | |
| ENST00000651160.1:c.1107A>G | ENSP00000498829.1:p.Ser369= | |
| ENST00000651541.1:c.810A>G | ENSP00000498795.1:p.Ser270= | |
| ENST00000651658.1:n.1534A>G | ||
| ENST00000651723.1:c.*1190A>G | ENSP00000498237.1:n.*1190A>G | |
| ENST00000652016.1:c.1107A>G | ENSP00000498267.1:p.Ser369= | |
| ENST00000652485.1:c.1107A>G | ENSP00000498973.1:p.Ser369= | |
| ENST00000378823.7:c.1107A>G | ENSP00000368100.4:p.Ser369= | |
| ENST00000423956.5:c.1107A>G | ENSP00000390971.1:p.Ser369= | |
| ENST00000453394.5:c.1107A>G | ENSP00000400049.1:p.Ser369= | |
| ENST00000487596.1:n.673A>G | ||
| ENST00000533482.5:c.*733A>G | ENSP00000431225.1:n.*733A>G | |
| NM_005732.3:c.1107A>G | NP_005723.2:p.Ser369= | |
| NM_005732.4:c.1107A>G MANE Select | NP_005723.2:p.Ser369= |