Canonical Allele Identifier: CA5617017
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs779113278
ExAC: 10:96701922 TC / T
gnomAD v2: 10-96701922-TC-T
gnomAD v3: 10-94942165-TC-T
gnomAD v4: 10-94942165-TC-T
MyVariant Identifiers: chr10:g.96701923del (hg19) chr10:g.94942166del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942167del , CM000672.2:g.94942167del GRCh38
NC_000010.10:g.96701924del , CM000672.1:g.96701924del GRCh37
NC_000010.9:g.96691914del NCBI36
NG_008385.1:g.8510del
NG_008385.2:g.9010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-25del MANE Select ENSP00000260682.6:n.332-25del
ENST00000643112.1:c.332-25del ENSP00000496202.1:n.332-25del
ENST00000645207.1:n.485-25del
ENST00000260682.6:c.332-25del ENSP00000260682.6:n.332-25del
ENST00000461906.1:n.357-25del
ENST00000473496.1:n.103-25del
NM_000771.3:c.332-25del NP_000762.2:n.332-25del
NM_000771.4:c.332-25del MANE Select NP_000762.2:n.332-25del
Search 100 bp 5'
Search 100 bp 3'