Canonical Allele Identifier: CA1929218635
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775201_94775203delinsAAG , CM000672.2:g.94775201_94775203delinsAAG GRCh38
NC_000010.10:g.96534958_96534960delinsAAG , CM000672.1:g.96534958_96534960delinsAAG GRCh37
NC_000010.9:g.96524948_96524950delinsAAG NCBI36
NG_008384.2:g.17496_17498delinsAAG
NG_008384.3:g.17521_17523delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.312_314delinsAAG MANE Select ENSP00000360372.3:p.Glu104=
ENST00000645461.1:n.1365_1367delinsAAG
ENST00000371321.7:c.312_314delinsAAG ENSP00000360372.3:p.Glu104=
ENST00000464755.1:c.1075_1077delinsAAG ENSP00000483243.1:n.1075_1077delinsAAG
ENST00000480405.2:c.312_314delinsAAG ENSP00000483847.1:p.Glu104=
NM_000769.2:c.312_314delinsAAG NP_000760.1:p.Glu104=
NM_000769.4:c.312_314delinsAAG MANE Select NP_000760.1:p.Glu104=
Search 100 bp 5'
Search 100 bp 3'