Canonical Allele Identifier: CA470836698
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96741067C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981310C>G , CM000672.2:g.94981310C>G GRCh38
NC_000010.10:g.96741067C>G , CM000672.1:g.96741067C>G GRCh37
NC_000010.9:g.96731057C>G NCBI36
NG_008385.1:g.47653C>G
NG_008385.2:g.48153C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1089C>G MANE Select ENSP00000260682.6:p.Pro363=
ENST00000643112.1:c.*98C>G ENSP00000496202.1:n.*98C>G
ENST00000260682.6:c.1089C>G ENSP00000260682.6:p.Pro363=
NM_000771.3:c.1089C>G NP_000762.2:p.Pro363=
NM_000771.4:c.1089C>G MANE Select NP_000762.2:p.Pro363=
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