Canonical Allele Identifier: CA1929213573
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762679T= , CM000672.2:g.94762679T= GRCh38
NC_000010.10:g.96522436T= , CM000672.1:g.96522436T= GRCh37
NC_000010.9:g.96512426T= NCBI36
NG_008384.2:g.4974T=
NG_008384.3:g.4999T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-27T= ENSP00000360372.3:n.-27T=
ENST00000464755.1:c.932-12379T= ENSP00000483243.1:n.932-12379T=