Canonical Allele Identifier: CA211729639
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs746068127
gnomAD v4: 10-94981218-A-G
COSMIC: COSM6028489
MyVariant Identifiers: chr10:g.96740975A>G (hg19) chr10:g.94981218A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981218A>G , CM000672.2:g.94981218A>G GRCh38
NC_000010.10:g.96740975A>G , CM000672.1:g.96740975A>G GRCh37
NC_000010.9:g.96730965A>G NCBI36
NG_008385.1:g.47561A>G
NG_008385.2:g.48061A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.997A>G MANE Select ENSP00000260682.6:p.Arg333Gly
ENST00000643112.1:c.*6A>G ENSP00000496202.1:n.*6A>G
ENST00000260682.6:c.997A>G ENSP00000260682.6:p.Arg333Gly
NM_000771.3:c.997A>G NP_000762.2:p.Arg333Gly
NM_000771.4:c.997A>G MANE Select NP_000762.2:p.Arg333Gly
Search 100 bp 5'
Search 100 bp 3'