Canonical Allele Identifier: CA211666129
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs151265892

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762629C>T , CM000672.2:g.94762629C>T GRCh38
NC_000010.10:g.96522386C>T , CM000672.1:g.96522386C>T GRCh37
NC_000010.9:g.96512376C>T NCBI36
NG_008384.2:g.4924C>T
NG_008384.3:g.4949C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-77C>T ENSP00000360372.3:n.-77C>T
ENST00000464755.1:c.932-12429C>T ENSP00000483243.1:n.932-12429C>T