Canonical Allele Identifier: CA1929213525
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762646G= , CM000672.2:g.94762646G= GRCh38
NC_000010.10:g.96522403G= , CM000672.1:g.96522403G= GRCh37
NC_000010.9:g.96512393G= NCBI36
NG_008384.2:g.4941G=
NG_008384.3:g.4966G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-60G= ENSP00000360372.3:n.-60G=
ENST00000464755.1:c.932-12412G= ENSP00000483243.1:n.932-12412G=