Canonical Allele Identifier: CA1929280002
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852995C= , CM000672.2:g.94852995C= GRCh38
NC_000010.10:g.96612752C= , CM000672.1:g.96612752C= GRCh37
NC_000010.9:g.96602742C= NCBI36
NG_008384.2:g.95290C=
NG_008384.3:g.95315C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*81C= MANE Select ENSP00000360372.3:n.*81C=
ENST00000645461.1:n.2465C=
ENST00000371321.7:c.*81C= ENSP00000360372.3:n.*81C=
ENST00000464755.1:c.2317C= ENSP00000483243.1:n.2317C=
NM_000769.2:c.*81C= NP_000760.1:n.*81C=
NM_000769.4:c.*81C= MANE Select NP_000760.1:n.*81C=
Search 100 bp 5'
Search 100 bp 3'