Linked Data
ClinVar Variation Id:
1562791
ClinVar RCV Id:
RCV002205065
dbSNP Id:
rs2145072224
MyVariant Identifiers:
chr17:g.37821648G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665395G>A , CM000679.2:g.39665395G>A | GRCh38 |
| NC_000017.10:g.37821648G>A , CM000679.1:g.37821648G>A | GRCh37 |
| NC_000017.9:g.35075174G>A | NCBI36 |
| NG_008892.1:g.5050G>A , LRG_210:g.5050G>A | |
| NG_042278.1:g.2415G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.36G>A MANE Select | ENSP00000312624.2:p.Glu12= | |
| ENST00000309889.2:c.36G>A | ENSP00000312624.2:p.Glu12= | |
| ENST00000578283.1:c.36G>A | ENSP00000462787.1:p.Glu12= | |
| NM_003673.3:c.36G>A , LRG_210t1:c.36G>A | NP_003664.1:p.Glu12= | |
| NM_003673.4:c.36G>A MANE Select | NP_003664.1:p.Glu12= |