Canonical Allele Identifier: CA1929279975
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852944G= , CM000672.2:g.94852944G= GRCh38
NC_000010.10:g.96612701G= , CM000672.1:g.96612701G= GRCh37
NC_000010.9:g.96602691G= NCBI36
NG_008384.2:g.95239G=
NG_008384.3:g.95264G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*30G= MANE Select ENSP00000360372.3:n.*30G=
ENST00000645461.1:n.2414G=
ENST00000371321.7:c.*30G= ENSP00000360372.3:n.*30G=
ENST00000464755.1:c.2266G= ENSP00000483243.1:n.2266G=
NM_000769.2:c.*30G= NP_000760.1:n.*30G=
NM_000769.4:c.*30G= MANE Select NP_000760.1:n.*30G=