Canonical Allele Identifier: CA595638664
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1184265943
gnomAD v2: 10-96541970-TA-T
gnomAD v3: 10-94782213-TA-T
gnomAD v4: 10-94782213-TA-T
MyVariant Identifiers: chr10:g.96541971del (hg19) chr10:g.94782214del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782216del , CM000672.2:g.94782216del GRCh38
NC_000010.10:g.96541973del , CM000672.1:g.96541973del GRCh37
NC_000010.9:g.96531963del NCBI36
NG_008384.2:g.24511del
NG_008384.3:g.24536del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+219del MANE Select ENSP00000360372.3:n.819+219del
ENST00000645461.1:n.1872+219del
ENST00000371321.7:c.819+219del ENSP00000360372.3:n.819+219del
ENST00000464755.1:c.1582+219del ENSP00000483243.1:n.1582+219del
NM_000769.2:c.819+219del NP_000760.1:n.819+219del
NM_000769.4:c.819+219del MANE Select NP_000760.1:n.819+219del
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