Canonical Allele Identifier: CA595321714
Gene: CYP2C9 HGNC NCBI

Linked Data

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

HGVS Genome Assembly
NC_000010.11:g.94974534del , CM000672.2:g.94974534del GRCh38
NC_000010.10:g.96734291del , CM000672.1:g.96734291del GRCh37
NC_000010.9:g.96724281del NCBI36
NG_008385.1:g.40877del
NG_008385.2:g.41377del

Transcript Alleles

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