Canonical Allele Identifier: CA5616484
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs140278421

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780574G>A , CM000672.2:g.94780574G>A GRCh38
NC_000010.10:g.96540331G>A , CM000672.1:g.96540331G>A GRCh37
NC_000010.9:g.96530321G>A NCBI36
NG_008384.2:g.22869G>A
NG_008384.3:g.22894G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.557G>A MANE Select ENSP00000360372.3:p.Arg186His
ENST00000645461.1:n.1610G>A
ENST00000371321.7:c.557G>A ENSP00000360372.3:p.Arg186His
ENST00000464755.1:n.1320G>A ENSP00000483243.1:p.=
NM_000769.2:c.557G>A NP_000760.1:p.Arg186His
NM_000769.4:c.557G>A MANE Select NP_000760.1:p.Arg186His