Canonical Allele Identifier: CA1929279922
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852837G= , CM000672.2:g.94852837G= GRCh38
NC_000010.10:g.96612594G= , CM000672.1:g.96612594G= GRCh37
NC_000010.9:g.96602584G= NCBI36
NG_008384.2:g.95132G=
NG_008384.3:g.95157G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1396G= MANE Select ENSP00000360372.3:p.Asp466=
ENST00000645461.1:n.2307G=
ENST00000371321.7:c.1396G= ENSP00000360372.3:p.Asp466=
ENST00000464755.1:c.2159G= ENSP00000483243.1:n.2159G=
NM_000769.2:c.1396G= NP_000760.1:p.Asp466=
NM_000769.4:c.1396G= MANE Select NP_000760.1:p.Asp466=