Canonical Allele Identifier: CA211735771
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs945634152
MyVariant Identifiers: chr10:g.96748867G>A (hg19) chr10:g.94989110G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989110G>A , CM000672.2:g.94989110G>A GRCh38
NC_000010.10:g.96748867G>A , CM000672.1:g.96748867G>A GRCh37
NC_000010.9:g.96738857G>A NCBI36
NG_008385.1:g.55453G>A
NG_008385.2:g.55953G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*82G>A MANE Select ENSP00000260682.6:n.*82G>A
ENST00000643112.1:c.*564G>A ENSP00000496202.1:n.*564G>A
ENST00000260682.6:c.*82G>A ENSP00000260682.6:n.*82G>A
NM_000771.3:c.*82G>A NP_000762.2:n.*82G>A
NM_000771.4:c.*82G>A MANE Select NP_000762.2:n.*82G>A
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