Canonical Allele Identifier: CA595638814
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1251925706
gnomAD v2: 10-96701918-TC-T
gnomAD v4: 10-94942161-TC-T
MyVariant Identifiers: chr10:g.96701919del (hg19) chr10:g.94942162del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942164del , CM000672.2:g.94942164del GRCh38
NC_000010.10:g.96701921del , CM000672.1:g.96701921del GRCh37
NC_000010.9:g.96691911del NCBI36
NG_008385.1:g.8507del
NG_008385.2:g.9007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-28del MANE Select ENSP00000260682.6:n.332-28del
ENST00000643112.1:c.332-28del ENSP00000496202.1:n.332-28del
ENST00000645207.1:n.485-28del
ENST00000260682.6:c.332-28del ENSP00000260682.6:n.332-28del
ENST00000461906.1:n.357-28del
ENST00000473496.1:n.103-28del
NM_000771.3:c.332-28del NP_000762.2:n.332-28del
NM_000771.4:c.332-28del MANE Select NP_000762.2:n.332-28del
Search 100 bp 5'
Search 100 bp 3'