Linked Data
ClinVar Variation Id:
856914
ClinVar RCV Id:
RCV001062482
dbSNP Id:
rs267606684
MyVariant Identifiers:
chr20:g.746025G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.765381G>T , CM000682.2:g.765381G>T | GRCh38 |
| NC_000020.10:g.746025G>T , CM000682.1:g.746025G>T | GRCh37 |
| NC_000020.9:g.694025G>T | NCBI36 |
| NG_027687.1:g.8204C>A | |
| NG_027687.2:g.15605C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381944.5:c.394C>A | ENSP00000371370.3:p.Arg132= | |
| ENST00000473664.2:c.394C>A | ENSP00000502741.1:p.Arg132= | |
| ENST00000488495.3:c.394C>A | ENSP00000494009.1:p.Arg132= | |
| ENST00000645534.1:c.394C>A MANE Select | ENSP00000494193.1:p.Arg132= | |
| ENST00000675066.1:c.394C>A | ENSP00000501902.1:p.Arg132= | |
| ENST00000676154.1:c.394C>A | ENSP00000501807.1:p.Arg132= | |
| ENST00000217254.11:c.394C>A | ENSP00000217254.7:p.Arg132= | |
| ENST00000381944.4:c.394C>A | ENSP00000371370.3:p.Arg132= | |
| ENST00000473664.1:n.445C>A | ||
| ENST00000632431.1:c.394C>A | ENSP00000488723.1:p.Arg132= | |
| NM_033409.3:c.394C>A | NP_212134.3:p.Arg132= | |
| XM_005260655.3:c.394C>A | XP_005260712.1:p.Arg132= | |
| XM_011529148.1:c.394C>A | XP_011527450.1:p.Arg132= | |
| XM_005260655.4:c.394C>A | XP_005260712.1:p.Arg132= | |
| XM_024451821.1:c.394C>A | XP_024307589.1:p.Arg132= | |
| NM_033409.4:c.394C>A MANE Select | NP_212134.3:p.Arg132= | |
| NM_001370085.1:c.394C>A | NP_001357014.1:p.Arg132= | |
| NM_001370086.1:c.394C>A | NP_001357015.1:p.Arg132= |