Linked Data
ClinVar Variation Id:
1565477
ClinVar RCV Id:
RCV002205334
dbSNP Id:
rs2128837713
MyVariant Identifiers:
chr8:g.19809429G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951918G>A , CM000670.2:g.19951918G>A | GRCh38 |
| NC_000008.10:g.19809429G>A , CM000670.1:g.19809429G>A | GRCh37 |
| NC_000008.9:g.19853709G>A | NCBI36 |
| NG_008855.1:g.17848G>A | |
| NG_008855.2:g.55202G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.399G>A MANE Select | ENSP00000497642.1:p.Gln133= | |
| ENST00000311322.8:c.399G>A | ENSP00000309757.6:p.Gln133= | |
| ENST00000520959.5:c.171G>A | ENSP00000428496.1:p.Gln57= | |
| NM_000237.2:c.399G>A | NP_000228.1:p.Gln133= | |
| NM_000237.3:c.399G>A MANE Select | NP_000228.1:p.Gln133= |