Canonical Allele Identifier: CA931378378
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v3: 10-94782262-G-GA
gnomAD v4: 10-94782262-G-GA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782262_94782263insA , CM000672.2:g.94782262_94782263insA GRCh38
NC_000010.10:g.96542019_96542020insA , CM000672.1:g.96542019_96542020insA GRCh37
NC_000010.9:g.96532009_96532010insA NCBI36
NG_008384.2:g.24557_24558insA
NG_008384.3:g.24582_24583insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+265_819+266insA MANE Select ENSP00000360372.3:n.819+265_819+266insA
ENST00000645461.1:n.1872+265_1872+266insA
ENST00000371321.7:c.819+265_819+266insA ENSP00000360372.3:n.819+265_819+266insA
ENST00000464755.1:c.1582+265_1582+266insA ENSP00000483243.1:n.1582+265_1582+266insA
NM_000769.2:c.819+265_819+266insA NP_000760.1:n.819+265_819+266insA
NM_000769.4:c.819+265_819+266insA MANE Select NP_000760.1:n.819+265_819+266insA
Search 100 bp 5'
Search 100 bp 3'