Canonical Allele Identifier: CA1929213561
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762674C= , CM000672.2:g.94762674C= GRCh38
NC_000010.10:g.96522431C= , CM000672.1:g.96522431C= GRCh37
NC_000010.9:g.96512421C= NCBI36
NG_008384.2:g.4969C=
NG_008384.3:g.4994C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-32C= ENSP00000360372.3:n.-32C=
ENST00000464755.1:c.932-12384C= ENSP00000483243.1:n.932-12384C=