Canonical Allele Identifier: CA1929213507
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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