Canonical Allele Identifier: CA595638650
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1215559432
gnomAD v2: 10-96541537-AT-A
gnomAD v4: 10-94781780-AT-A
MyVariant Identifiers: chr10:g.96541538del (hg19) chr10:g.94781781del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781782del , CM000672.2:g.94781782del GRCh38
NC_000010.10:g.96541539del , CM000672.1:g.96541539del GRCh37
NC_000010.9:g.96531529del NCBI36
NG_008384.2:g.24077del
NG_008384.3:g.24102del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-39del MANE Select ENSP00000360372.3:n.643-39del
ENST00000645461.1:n.1696-39del
ENST00000371321.7:c.643-39del ENSP00000360372.3:n.643-39del
ENST00000464755.1:c.1406-39del ENSP00000483243.1:n.1406-39del
NM_000769.2:c.643-39del NP_000760.1:n.643-39del
NM_000769.4:c.643-39del MANE Select NP_000760.1:n.643-39del
Search 100 bp 5'
Search 100 bp 3'