Canonical Allele Identifier: CA2610265348
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853060-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853066del , CM000672.2:g.94853066del GRCh38
NC_000010.10:g.96612823del , CM000672.1:g.96612823del GRCh37
NC_000010.9:g.96602813del NCBI36
NG_008384.2:g.95361del
NG_008384.3:g.95386del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*152del MANE Select ENSP00000360372.3:n.*152del
ENST00000645461.1:n.2536del
ENST00000371321.7:c.*152del ENSP00000360372.3:n.*152del
ENST00000464755.1:c.2388del ENSP00000483243.1:n.2388del
NM_000769.2:c.*152del NP_000760.1:n.*152del
NM_000769.4:c.*152del MANE Select NP_000760.1:n.*152del
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