Canonical Allele Identifier: CA1929278306
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850020A= , CM000672.2:g.94850020A= GRCh38
NC_000010.10:g.96609777A= , CM000672.1:g.96609777A= GRCh37
NC_000010.9:g.96599767A= NCBI36
NG_008384.2:g.92315A=
NG_008384.3:g.92340A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1253A= MANE Select ENSP00000360372.3:p.Asn418=
ENST00000645461.1:n.2164A=
ENST00000371321.7:c.1253A= ENSP00000360372.3:p.Asn418=
ENST00000464755.1:c.2016A= ENSP00000483243.1:n.2016A=
NM_000769.2:c.1253A= NP_000760.1:p.Asn418=
NM_000769.4:c.1253A= MANE Select NP_000760.1:p.Asn418=