Linked Data
ClinVar Variation Id:
1533275
ClinVar RCV Id:
RCV002102302
dbSNP Id:
rs752713602
MyVariant Identifiers:
chr3:g.120352102C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.120633255C>G , CM000665.2:g.120633255C>G | GRCh38 |
| NC_000003.11:g.120352102C>G , CM000665.1:g.120352102C>G | GRCh37 |
| NC_000003.10:g.121834792C>G | NCBI36 |
| NG_011957.1:g.54227G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000283871.10:c.1080G>C MANE Select | ENSP00000283871.5:p.Gly360= | |
| ENST00000283871.9:c.1080G>C | ENSP00000283871.5:p.Gly360= | |
| ENST00000470321.1:n.420G>C | ||
| ENST00000492108.5:c.359G>C | ENSP00000419838.1:n.359G>C | |
| NM_000187.3:c.1080G>C | NP_000178.2:p.Gly360= | |
| XM_005247412.1:c.855G>C | XP_005247469.1:p.Gly285= | |
| XM_005247412.2:c.855G>C | XP_005247469.1:p.Gly285= | |
| XM_017006277.2:c.657G>C | XP_016861766.1:p.Gly219= | |
| NM_000187.4:c.1080G>C MANE Select | NP_000178.2:p.Gly360= |