Canonical Allele Identifier: CA2610265277
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852987-CTG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852990_94852991del , CM000672.2:g.94852990_94852991del GRCh38
NC_000010.10:g.96612747_96612748del , CM000672.1:g.96612747_96612748del GRCh37
NC_000010.9:g.96602737_96602738del NCBI36
NG_008384.2:g.95285_95286del
NG_008384.3:g.95310_95311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*76_*77del MANE Select ENSP00000360372.3:n.*76_*77del
ENST00000645461.1:n.2460_2461del
ENST00000371321.7:c.*76_*77del ENSP00000360372.3:n.*76_*77del
ENST00000464755.1:c.2312_2313del ENSP00000483243.1:n.2312_2313del
NM_000769.2:c.*76_*77del NP_000760.1:n.*76_*77del
NM_000769.4:c.*76_*77del MANE Select NP_000760.1:n.*76_*77del
Search 100 bp 5'
Search 100 bp 3'