Canonical Allele Identifier: CA1929218721
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848392672

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775345_94775346insAGCT , CM000672.2:g.94775345_94775346insAGCT GRCh38
NC_000010.10:g.96535102_96535103insAGCT , CM000672.1:g.96535102_96535103insAGCT GRCh37
NC_000010.9:g.96525092_96525093insAGCT NCBI36
NG_008384.2:g.17640_17641insAGCT
NG_008384.3:g.17665_17666insAGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.332-45_332-44insAGCT MANE Select ENSP00000360372.3:n.332-45_332-44insAGCT
ENST00000645461.1:n.1385-45_1385-44insAGCT
ENST00000371321.7:c.332-45_332-44insAGCT ENSP00000360372.3:n.332-45_332-44insAGCT
ENST00000464755.1:c.1095-45_1095-44insAGCT ENSP00000483243.1:n.1095-45_1095-44insAGC...
ENST00000480405.2:c.332-45_332-44insAGCT ENSP00000483847.1:n.332-45_332-44insAGCT
NM_000769.2:c.332-45_332-44insAGCT NP_000760.1:n.332-45_332-44insAGCT
NM_000769.4:c.332-45_332-44insAGCT MANE Select NP_000760.1:n.332-45_332-44insAGCT