Canonical Allele Identifier: CA1929213484
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762629C= , CM000672.2:g.94762629C= GRCh38
NC_000010.10:g.96522386C= , CM000672.1:g.96522386C= GRCh37
NC_000010.9:g.96512376C= NCBI36
NG_008384.2:g.4924C=
NG_008384.3:g.4949C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-77C= ENSP00000360372.3:n.-77C=
ENST00000464755.1:c.932-12429C= ENSP00000483243.1:n.932-12429C=