Canonical Allele Identifier: CA1929280010
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853015C= , CM000672.2:g.94853015C= GRCh38
NC_000010.10:g.96612772C= , CM000672.1:g.96612772C= GRCh37
NC_000010.9:g.96602762C= NCBI36
NG_008384.2:g.95310C=
NG_008384.3:g.95335C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*101C= MANE Select ENSP00000360372.3:n.*101C=
ENST00000645461.1:n.2485C=
ENST00000371321.7:c.*101C= ENSP00000360372.3:n.*101C=
ENST00000464755.1:c.2337C= ENSP00000483243.1:n.2337C=
NM_000769.2:c.*101C= NP_000760.1:n.*101C=
NM_000769.4:c.*101C= MANE Select NP_000760.1:n.*101C=