Canonical Allele Identifier: CA2610267816
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94942390-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942390T>A , CM000672.2:g.94942390T>A GRCh38
NC_000010.10:g.96702147T>A , CM000672.1:g.96702147T>A GRCh37
NC_000010.9:g.96692137T>A NCBI36
NG_008385.1:g.8733T>A
NG_008385.2:g.9233T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+49T>A MANE Select ENSP00000260682.6:n.481+49T>A
ENST00000643112.1:c.481+49T>A ENSP00000496202.1:n.481+49T>A
ENST00000645207.1:n.634+49T>A
ENST00000260682.6:c.481+49T>A ENSP00000260682.6:n.481+49T>A
ENST00000461906.1:n.555T>A
ENST00000473496.1:n.252+49T>A
NM_000771.3:c.481+49T>A NP_000762.2:n.481+49T>A
NM_000771.4:c.481+49T>A MANE Select NP_000762.2:n.481+49T>A
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