Canonical Allele Identifier: CA470832041
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540317T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780560T>C , CM000672.2:g.94780560T>C GRCh38
NC_000010.10:g.96540317T>C , CM000672.1:g.96540317T>C GRCh37
NC_000010.9:g.96530307T>C NCBI36
NG_008384.2:g.22855T>C
NG_008384.3:g.22880T>C

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.543T>C NP_000760.1:p.Ile181=
NM_000769.4:c.543T>C MANE Select NP_000760.1:p.Ile181=
ENST00000371321.7:c.543T>C ENSP00000360372.3:p.Ile181=
ENST00000464755.1:n.1306T>C ENSP00000483243.1:p.=