Canonical Allele Identifier: CA2574622143
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762640C>A , CM000672.2:g.94762640C>A GRCh38
NC_000010.10:g.96522397C>A , CM000672.1:g.96522397C>A GRCh37
NC_000010.9:g.96512387C>A NCBI36
NG_008384.2:g.4935C>A
NG_008384.3:g.4960C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-66C>A ENSP00000360372.3:n.-66C>A
ENST00000464755.1:c.932-12418C>A ENSP00000483243.1:n.932-12418C>A