Canonical Allele Identifier: CA2610266858
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94989103-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989103A>G , CM000672.2:g.94989103A>G GRCh38
NC_000010.10:g.96748860A>G , CM000672.1:g.96748860A>G GRCh37
NC_000010.9:g.96738850A>G NCBI36
NG_008385.1:g.55446A>G
NG_008385.2:g.55946A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*75A>G MANE Select ENSP00000260682.6:n.*75A>G
ENST00000643112.1:c.*557A>G ENSP00000496202.1:n.*557A>G
ENST00000260682.6:c.*75A>G ENSP00000260682.6:n.*75A>G
NM_000771.3:c.*75A>G NP_000762.2:n.*75A>G
NM_000771.4:c.*75A>G MANE Select NP_000762.2:n.*75A>G
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