Canonical Allele Identifier: CA2610266842
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94989055-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989055T>C , CM000672.2:g.94989055T>C GRCh38
NC_000010.10:g.96748812T>C , CM000672.1:g.96748812T>C GRCh37
NC_000010.9:g.96738802T>C NCBI36
NG_008385.1:g.55398T>C
NG_008385.2:g.55898T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*27T>C MANE Select ENSP00000260682.6:n.*27T>C
ENST00000643112.1:c.*509T>C ENSP00000496202.1:n.*509T>C
ENST00000260682.6:c.*27T>C ENSP00000260682.6:n.*27T>C
NM_000771.3:c.*27T>C NP_000762.2:n.*27T>C
NM_000771.4:c.*27T>C MANE Select NP_000762.2:n.*27T>C
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