Canonical Allele Identifier: CA670191443

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1474696545
• MyVariant Identifiers: chr10:g.96522395A>C (hg19) ; chr10:g.94762638A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762638A>C , CM000672.2:g.94762638A>C	GRCh38
NC_000010.10:g.96522395A>C , CM000672.1:g.96522395A>C	GRCh37
NC_000010.9:g.96512385A>C	NCBI36
NG_008384.2:g.4933A>C
NG_008384.3:g.4958A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.7:c.-68A>C	ENSP00000360372.3:n.-68A>C
ENST00000464755.1:c.932-12420A>C	ENSP00000483243.1:n.932-12420A>C