Canonical Allele Identifier: CA1929213574

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1589815047

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762679T>C , CM000672.2:g.94762679T>C	GRCh38
NC_000010.10:g.96522436T>C , CM000672.1:g.96522436T>C	GRCh37
NC_000010.9:g.96512426T>C	NCBI36
NG_008384.2:g.4974T>C
NG_008384.3:g.4999T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.7:c.-27T>C	ENSP00000360372.3:n.-27T>C
ENST00000464755.1:c.932-12379T>C	ENSP00000483243.1:n.932-12379T>C