Canonical Allele Identifier: CA211680925
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs945712113

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780524C>A , CM000672.2:g.94780524C>A GRCh38
NC_000010.10:g.96540281C>A , CM000672.1:g.96540281C>A GRCh37
NC_000010.9:g.96530271C>A NCBI36
NG_008384.2:g.22819C>A
NG_008384.3:g.22844C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.507C>A MANE Select ENSP00000360372.3:p.Ile169=
ENST00000645461.1:n.1560C>A
ENST00000371321.7:c.507C>A ENSP00000360372.3:p.Ile169=
ENST00000464755.1:c.1270C>A ENSP00000483243.1:n.1270C>A
NM_000769.2:c.507C>A NP_000760.1:p.Ile169=
NM_000769.4:c.507C>A MANE Select NP_000760.1:p.Ile169=