Canonical Allele Identifier: CA2610265303
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853018-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853022del , CM000672.2:g.94853022del GRCh38
NC_000010.10:g.96612779del , CM000672.1:g.96612779del GRCh37
NC_000010.9:g.96602769del NCBI36
NG_008384.2:g.95317del
NG_008384.3:g.95342del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*108del MANE Select ENSP00000360372.3:n.*108del
ENST00000645461.1:n.2492del
ENST00000371321.7:c.*108del ENSP00000360372.3:n.*108del
ENST00000464755.1:c.2344del ENSP00000483243.1:n.2344del
NM_000769.2:c.*108del NP_000760.1:n.*108del
NM_000769.4:c.*108del MANE Select NP_000760.1:n.*108del
Search 100 bp 5'
Search 100 bp 3'