Canonical Allele Identifier: CA1929271596
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94842787A= , CM000672.2:g.94842787A= GRCh38
NC_000010.10:g.96602544A= , CM000672.1:g.96602544A= GRCh37
NC_000010.9:g.96592534A= NCBI36
NG_008384.2:g.85082A=
NG_008384.3:g.85107A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.962-50A= MANE Select ENSP00000360372.3:n.962-50A=
ENST00000645461.1:n.1873-50A=
ENST00000371321.7:c.962-50A= ENSP00000360372.3:n.962-50A=
ENST00000464755.1:c.1725-50A= ENSP00000483243.1:n.1725-50A=
NM_000769.2:c.962-50A= NP_000760.1:n.962-50A=
NM_000769.4:c.962-50A= MANE Select NP_000760.1:n.962-50A=