Canonical Allele Identifier: CA1929213567
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762677G= , CM000672.2:g.94762677G= GRCh38
NC_000010.10:g.96522434G= , CM000672.1:g.96522434G= GRCh37
NC_000010.9:g.96512424G= NCBI36
NG_008384.2:g.4972G=
NG_008384.3:g.4997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-29G= ENSP00000360372.3:n.-29G=
ENST00000464755.1:c.932-12381G= ENSP00000483243.1:n.932-12381G=