Canonical Allele Identifier: CA1929278264
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849959A= , CM000672.2:g.94849959A= GRCh38
NC_000010.10:g.96609716A= , CM000672.1:g.96609716A= GRCh37
NC_000010.9:g.96599706A= NCBI36
NG_008384.2:g.92254A=
NG_008384.3:g.92279A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1192A= MANE Select ENSP00000360372.3:p.Asn398=
ENST00000645461.1:n.2103A=
ENST00000371321.7:c.1192A= ENSP00000360372.3:p.Asn398=
ENST00000464755.1:c.1955A= ENSP00000483243.1:n.1955A=
NM_000769.2:c.1192A= NP_000760.1:p.Asn398=
NM_000769.4:c.1192A= MANE Select NP_000760.1:p.Asn398=