Canonical Allele Identifier: CA470987484
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701950A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942193A>G , CM000672.2:g.94942193A>G GRCh38
NC_000010.10:g.96701950A>G , CM000672.1:g.96701950A>G GRCh37
NC_000010.9:g.96691940A>G NCBI36
NG_008385.1:g.8536A>G
NG_008385.2:g.9036A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.333A>G MANE Select ENSP00000260682.6:p.Gly111=
ENST00000643112.1:c.333A>G ENSP00000496202.1:p.Gly111=
ENST00000645207.1:n.486A>G
ENST00000260682.6:c.333A>G ENSP00000260682.6:p.Gly111=
ENST00000461906.1:n.358A>G
ENST00000473496.1:n.104A>G
NM_000771.3:c.333A>G NP_000762.2:p.Gly111=
NM_000771.4:c.333A>G MANE Select NP_000762.2:p.Gly111=