Canonical Allele Identifier: CA931367420
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848185028

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762639G>T , CM000672.2:g.94762639G>T GRCh38
NC_000010.10:g.96522396G>T , CM000672.1:g.96522396G>T GRCh37
NC_000010.9:g.96512386G>T NCBI36
NG_008384.2:g.4934G>T
NG_008384.3:g.4959G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-67G>T ENSP00000360372.3:n.-67G>T
ENST00000464755.1:c.932-12419G>T ENSP00000483243.1:n.932-12419G>T