Canonical Allele Identifier: CA1929279992
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852976A= , CM000672.2:g.94852976A= GRCh38
NC_000010.10:g.96612733A= , CM000672.1:g.96612733A= GRCh37
NC_000010.9:g.96602723A= NCBI36
NG_008384.2:g.95271A=
NG_008384.3:g.95296A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*62A= MANE Select ENSP00000360372.3:n.*62A=
ENST00000645461.1:n.2446A=
ENST00000371321.7:c.*62A= ENSP00000360372.3:n.*62A=
ENST00000464755.1:c.2298A= ENSP00000483243.1:n.2298A=
NM_000769.2:c.*62A= NP_000760.1:n.*62A=
NM_000769.4:c.*62A= MANE Select NP_000760.1:n.*62A=