Canonical Allele Identifier: CA595321718
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1391938687
gnomAD v2: 10-96734283-A-ATT
gnomAD v3: 10-94974526-A-ATT
gnomAD v4: 10-94974526-A-ATT
MyVariant Identifiers: chr10:g.96734284_96734285insTT (hg19) chr10:g.94974527_94974528insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974533_94974534dup , CM000672.2:g.94974533_94974534dup GRCh38
NC_000010.10:g.96734290_96734291dup , CM000672.1:g.96734290_96734291dup GRCh37
NC_000010.9:g.96724280_96724281dup NCBI36
NG_008385.1:g.40876_40877dup
NG_008385.2:g.41376_41377dup

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.961+2288_961+2289dup MANE Select ENSP00000260682.6:n.961+2288_961+2289dup
ENST00000643112.1:c.820-6650_820-6649dup ENSP00000496202.1:n.820-6650_820-6649dup
ENST00000260682.6:c.961+2288_961+2289dup ENSP00000260682.6:n.961+2288_961+2289dup
NM_000771.3:c.961+2288_961+2289dup NP_000762.2:n.961+2288_961+2289dup
NM_000771.4:c.961+2288_961+2289dup MANE Select NP_000762.2:n.961+2288_961+2289dup
Search 100 bp 5'
Search 100 bp 3'