Canonical Allele Identifier: CA1929213489
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762631C= , CM000672.2:g.94762631C= GRCh38
NC_000010.10:g.96522388C= , CM000672.1:g.96522388C= GRCh37
NC_000010.9:g.96512378C= NCBI36
NG_008384.2:g.4926C=
NG_008384.3:g.4951C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-75C= ENSP00000360372.3:n.-75C=
ENST00000464755.1:c.932-12427C= ENSP00000483243.1:n.932-12427C=