Canonical Allele Identifier: CA2839209663
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989091T>C , CM000672.2:g.94989091T>C GRCh38
NC_000010.10:g.96748848T>C , CM000672.1:g.96748848T>C GRCh37
NC_000010.9:g.96738838T>C NCBI36
NG_008385.1:g.55434T>C
NG_008385.2:g.55934T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*63T>C MANE Select ENSP00000260682.6:n.*63T>C
ENST00000643112.1:c.*545T>C ENSP00000496202.1:n.*545T>C
ENST00000260682.6:c.*63T>C ENSP00000260682.6:n.*63T>C
NM_000771.3:c.*63T>C NP_000762.2:n.*63T>C
NM_000771.4:c.*63T>C MANE Select NP_000762.2:n.*63T>C
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