Canonical Allele Identifier: CA1929222191
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781702C= , CM000672.2:g.94781702C= GRCh38
NC_000010.10:g.96541459C= , CM000672.1:g.96541459C= GRCh37
NC_000010.9:g.96531449C= NCBI36
NG_008384.2:g.23997C=
NG_008384.3:g.24022C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.643-119C= MANE Select ENSP00000360372.3:n.643-119C=
ENST00000645461.1:n.1696-119C=
ENST00000371321.7:c.643-119C= ENSP00000360372.3:n.643-119C=
ENST00000464755.1:c.1406-119C= ENSP00000483243.1:n.1406-119C=
NM_000769.2:c.643-119C= NP_000760.1:n.643-119C=
NM_000769.4:c.643-119C= MANE Select NP_000760.1:n.643-119C=