Linked Data
ClinVar Variation Id:
2803074
ClinVar RCV Id:
RCV003620599
gnomAD v4:
20-10658667-C-A
MyVariant Identifiers:
chr20:g.10639315C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658667C>A , CM000682.2:g.10658667C>A | GRCh38 |
| NC_000020.10:g.10639315C>A , CM000682.1:g.10639315C>A | GRCh37 |
| NC_000020.9:g.10587315C>A | NCBI36 |
| NG_007496.1:g.20380G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.495G>T MANE Select | ENSP00000254958.4:p.Arg165= | |
| ENST00000254958.9:c.495G>T | ENSP00000254958.4:p.Arg165= | |
| ENST00000423891.6:n.361G>T | ||
| NM_000214.2:c.495G>T | NP_000205.1:p.Arg165= | |
| NM_000214.3:c.495G>T MANE Select | NP_000205.1:p.Arg165= |