Canonical Allele Identifier: CA1929213535
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762652T= , CM000672.2:g.94762652T= GRCh38
NC_000010.10:g.96522409T= , CM000672.1:g.96522409T= GRCh37
NC_000010.9:g.96512399T= NCBI36
NG_008384.2:g.4947T=
NG_008384.3:g.4972T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-54T= ENSP00000360372.3:n.-54T=
ENST00000464755.1:c.932-12406T= ENSP00000483243.1:n.932-12406T=