Canonical Allele Identifier: CA213564
Gene: CASR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 35778
ClinVar RCV Id: RCV000029430
dbSNP Id: rs193922423

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122275959G>A , CM000665.2:g.122275959G>A GRCh38
NC_000003.10:g.123477496G>A NCBI36
NC_000003.11:g.121994806G>A , CM000665.1:g.121994806G>A GRCh37
NG_009058.1:g.97277G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000490131.5:c.1525G>A ENSP00000418685.1:p.Gly509Arg
ENST00000498619.2:c.1525G>A ENSP00000420194.1:p.Gly509Arg
NM_000388.3:c.1525G>A VV NP_000379.2:p.Gly509Arg
NM_001178065.1:c.1525G>A VV NP_001171536.1:p.Gly509Arg
XM_005247836.2:c.1525G>A XP_005247893.1:p.Gly509Arg
XM_005247837.2:c.1042G>A XP_005247894.1:p.Gly348Arg
XM_006713789.2:c.1525G>A XP_006713852.1:p.Gly509Arg
XM_011513237.1:c.1525G>A XP_011511539.1:p.Gly509Arg
XM_011513238.1:c.1525G>A XP_011511540.1:p.Gly509Arg
XM_011513239.1:c.937G>A XP_011511541.1:p.Gly313Arg