Canonical Allele Identifier: CA5617270
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs776018319
ExAC: 10:96740949 A / G
gnomAD v2: 10-96740949-A-G
gnomAD v3: 10-94981192-A-G
gnomAD v4: 10-94981192-A-G
MyVariant Identifiers: chr10:g.96740949A>G (hg19) chr10:g.94981192A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981192A>G , CM000672.2:g.94981192A>G GRCh38
NC_000010.10:g.96740949A>G , CM000672.1:g.96740949A>G GRCh37
NC_000010.9:g.96730939A>G NCBI36
NG_008385.1:g.47535A>G
NG_008385.2:g.48035A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.971A>G MANE Select ENSP00000260682.6:p.Gln324Arg
ENST00000643112.1:c.829A>G ENSP00000496202.1:p.Arg277Gly
ENST00000260682.6:c.971A>G ENSP00000260682.6:p.Gln324Arg
NM_000771.3:c.971A>G NP_000762.2:p.Gln324Arg
NM_000771.4:c.971A>G MANE Select NP_000762.2:p.Gln324Arg
Search 100 bp 5'
Search 100 bp 3'