Canonical Allele Identifier: CA470832169

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96541580A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781823A>C , CM000672.2:g.94781823A>C	GRCh38
NC_000010.10:g.96541580A>C , CM000672.1:g.96541580A>C	GRCh37
NC_000010.9:g.96531570A>C	NCBI36
NG_008384.2:g.24118A>C
NG_008384.3:g.24143A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.645A>C MANE Select	ENSP00000360372.3:p.Ile215=
ENST00000645461.1:n.1698A>C
ENST00000371321.7:c.645A>C	ENSP00000360372.3:p.Ile215=
ENST00000464755.1:c.1408A>C	ENSP00000483243.1:n.1408A>C
NM_000769.2:c.645A>C	NP_000760.1:p.Ile215=
NM_000769.4:c.645A>C MANE Select	NP_000760.1:p.Ile215=