Canonical Allele Identifier: CA470832006
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540263C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780506C>A , CM000672.2:g.94780506C>A GRCh38
NC_000010.10:g.96540263C>A , CM000672.1:g.96540263C>A GRCh37
NC_000010.9:g.96530253C>A NCBI36
NG_008384.2:g.22801C>A
NG_008384.3:g.22826C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.489C>A MANE Select ENSP00000360372.3:p.Pro163=
ENST00000371321.7:c.489C>A ENSP00000360372.3:p.Pro163=
ENST00000464755.1:n.1252C>A ENSP00000483243.1:p.=
NM_000769.2:c.489C>A NP_000760.1:p.Pro163=
NM_000769.4:c.489C>A MANE Select NP_000760.1:p.Pro163=