Linked Data
ClinVar Variation Id:
38962
ClinVar RCV Id:
RCV002247408
dbSNP Id:
rs113994107
PubMed:
PMID:20301768
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110186513C>T , CM000675.2:g.110186513C>T | GRCh38 |
| NC_000013.10:g.110838860C>T , CM000675.1:g.110838860C>T | GRCh37 |
| NC_000013.9:g.109636861C>T | NCBI36 |
| NG_011544.2:g.125637G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375820.10:c.1769G>A MANE Select | ENSP00000364979.4:p.Gly590Glu | |
| ENST00000649738.1:n.1899G>A | ||
| ENST00000375820.8:c.1769G>A | ENSP00000364979.4:p.Gly590Glu | |
| NM_001845.5:c.1769G>A | NP_001836.3:p.Gly590Glu | |
| XM_011521048.1:c.1577G>A | XP_011519350.1:p.Gly526Glu | |
| XM_011521048.2:c.1577G>A | XP_011519350.1:p.Gly526Glu | |
| NM_001845.6:c.1769G>A MANE Select | NP_001836.3:p.Gly590Glu |