Canonical Allele Identifier: CA670161380
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1248307888
MyVariant Identifiers: chr10:g.96535148del (hg19) chr10:g.94775391del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775392del , CM000672.2:g.94775392del GRCh38
NC_000010.10:g.96535149del , CM000672.1:g.96535149del GRCh37
NC_000010.9:g.96525139del NCBI36
NG_008384.2:g.17687del
NG_008384.3:g.17712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.334del MANE Select ENSP00000360372.3:p.Ile112SerfsTer18
ENST00000645461.1:n.1387del
ENST00000371321.7:c.334del ENSP00000360372.3:p.Ile112SerfsTer18
ENST00000464755.1:c.1097del ENSP00000483243.1:n.1097del
ENST00000480405.2:c.334del ENSP00000483847.1:p.Ile112SerfsTer18
NM_000769.2:c.334del NP_000760.1:p.Ile112SerfsTer18
NM_000769.4:c.334del MANE Select NP_000760.1:p.Ile112SerfsTer18
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