Canonical Allele Identifier: CA2841724317
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762634A>G , CM000672.2:g.94762634A>G GRCh38
NC_000010.10:g.96522391A>G , CM000672.1:g.96522391A>G GRCh37
NC_000010.9:g.96512381A>G NCBI36
NG_008384.2:g.4929A>G
NG_008384.3:g.4954A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-72A>G ENSP00000360372.3:n.-72A>G
ENST00000464755.1:c.932-12424A>G ENSP00000483243.1:n.932-12424A>G