Linked Data
ClinVar Variation Id:
3008490
ClinVar RCV Id:
RCV003867153
dbSNP Id:
rs763798259
ExAC:
20:10629736 G / A
gnomAD v2:
20-10629736-G-A
gnomAD v3:
20-10649088-G-A
gnomAD v4:
20-10649088-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10649088G>A , CM000682.2:g.10649088G>A | GRCh38 |
| NC_000020.10:g.10629736G>A , CM000682.1:g.10629736G>A | GRCh37 |
| NC_000020.9:g.10577736G>A | NCBI36 |
| NG_007496.1:g.29959C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.1368C>T MANE Select | ENSP00000254958.4:p.Gly456= | |
| ENST00000617965.2:n.1957C>T | ||
| ENST00000254958.9:c.1368C>T | ENSP00000254958.4:p.Gly456= | |
| ENST00000423891.6:n.1234C>T | ||
| ENST00000620743.1:n.87C>T | ||
| ENST00000622545.1:c.145C>T | ||
| NM_000214.2:c.1368C>T | NP_000205.1:p.Gly456= | |
| NM_000214.3:c.1368C>T MANE Select | NP_000205.1:p.Gly456= |