Canonical Allele Identifier: CA470832280

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96541724T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781967T>C , CM000672.2:g.94781967T>C	GRCh38
NC_000010.10:g.96541724T>C , CM000672.1:g.96541724T>C	GRCh37
NC_000010.9:g.96531714T>C	NCBI36
NG_008384.2:g.24262T>C
NG_008384.3:g.24287T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.789T>C MANE Select	ENSP00000360372.3:p.Phe263=
ENST00000645461.1:n.1842T>C
ENST00000371321.7:c.789T>C	ENSP00000360372.3:p.Phe263=
ENST00000464755.1:c.1552T>C	ENSP00000483243.1:n.1552T>C
NM_000769.2:c.789T>C	NP_000760.1:p.Phe263=
NM_000769.4:c.789T>C MANE Select	NP_000760.1:p.Phe263=