Canonical Allele Identifier: CA377674248
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs776115064
gnomAD v2: 10-96708998-A-T
gnomAD v4: 10-94949241-A-T
MyVariant Identifiers: chr10:g.96708998A>T (hg19) chr10:g.94949241A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949241A>T , CM000672.2:g.94949241A>T GRCh38
NC_000010.10:g.96708998A>T , CM000672.1:g.96708998A>T GRCh37
NC_000010.9:g.96698988A>T NCBI36
NG_008385.1:g.15584A>T
NG_008385.2:g.16084A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.776A>T MANE Select ENSP00000260682.6:p.Asn259Ile
ENST00000643112.1:c.776A>T ENSP00000496202.1:p.Asn259Ile
ENST00000260682.6:c.776A>T ENSP00000260682.6:p.Asn259Ile
ENST00000473496.1:n.547A>T
NM_000771.3:c.776A>T NP_000762.2:p.Asn259Ile
NM_000771.4:c.776A>T MANE Select NP_000762.2:p.Asn259Ile
Search 100 bp 5'
Search 100 bp 3'