Canonical Allele Identifier: CA1929279960
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852924G= , CM000672.2:g.94852924G= GRCh38
NC_000010.10:g.96612681G= , CM000672.1:g.96612681G= GRCh37
NC_000010.9:g.96602671G= NCBI36
NG_008384.2:g.95219G=
NG_008384.3:g.95244G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*10G= MANE Select ENSP00000360372.3:n.*10G=
ENST00000645461.1:n.2394G=
ENST00000371321.7:c.*10G= ENSP00000360372.3:n.*10G=
ENST00000464755.1:c.2246G= ENSP00000483243.1:n.2246G=
NM_000769.2:c.*10G= NP_000760.1:n.*10G=
NM_000769.4:c.*10G= MANE Select NP_000760.1:n.*10G=