Canonical Allele Identifier: CA1929218770
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775426_94775427delinsTC , CM000672.2:g.94775426_94775427delinsTC GRCh38
NC_000010.10:g.96535183_96535184delinsTC , CM000672.1:g.96535183_96535184delinsTC GRCh37
NC_000010.9:g.96525173_96525174delinsTC NCBI36
NG_008384.2:g.17721_17722delinsTC
NG_008384.3:g.17746_17747delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.368_369delinsTC MANE Select ENSP00000360372.3:p.Ile123=
ENST00000645461.1:n.1421_1422delinsTC
ENST00000371321.7:c.368_369delinsTC ENSP00000360372.3:p.Ile123=
ENST00000464755.1:c.1131_1132delinsTC ENSP00000483243.1:n.1131_1132delinsTC
ENST00000480405.2:c.368_369delinsTC ENSP00000483847.1:p.Ile123=
NM_000769.2:c.368_369delinsTC NP_000760.1:p.Ile123=
NM_000769.4:c.368_369delinsTC MANE Select NP_000760.1:p.Ile123=
Search 100 bp 5'
Search 100 bp 3'