Canonical Allele Identifier: CA470837360
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032364780
MyVariant Identifiers: chr10:g.96748626A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988869A>G , CM000672.2:g.94988869A>G GRCh38
NC_000010.10:g.96748626A>G , CM000672.1:g.96748626A>G GRCh37
NC_000010.9:g.96738616A>G NCBI36
NG_008385.1:g.55212A>G
NG_008385.2:g.55712A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1314A>G MANE Select ENSP00000260682.6:p.Glu438=
ENST00000643112.1:c.*323A>G ENSP00000496202.1:n.*323A>G
ENST00000260682.6:c.1314A>G ENSP00000260682.6:p.Glu438=
NM_000771.3:c.1314A>G NP_000762.2:p.Glu438=
NM_000771.4:c.1314A>G MANE Select NP_000762.2:p.Glu438=