Canonical Allele Identifier: CA1929213571
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762678G= , CM000672.2:g.94762678G= GRCh38
NC_000010.10:g.96522435G= , CM000672.1:g.96522435G= GRCh37
NC_000010.9:g.96512425G= NCBI36
NG_008384.2:g.4973G=
NG_008384.3:g.4998G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-28G= ENSP00000360372.3:n.-28G=
ENST00000464755.1:c.932-12380G= ENSP00000483243.1:n.932-12380G=