Canonical Allele Identifier: CA2528783860
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94942047-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942047A>T , CM000672.2:g.94942047A>T GRCh38
NC_000010.10:g.96701804A>T , CM000672.1:g.96701804A>T GRCh37
NC_000010.9:g.96691794A>T NCBI36
NG_008385.1:g.8390A>T
NG_008385.2:g.8890A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.331+27A>T MANE Select ENSP00000260682.6:n.331+27A>T
ENST00000643112.1:c.331+27A>T ENSP00000496202.1:n.331+27A>T
ENST00000645207.1:n.484+27A>T
ENST00000260682.6:c.331+27A>T ENSP00000260682.6:n.331+27A>T
ENST00000461906.1:n.356+27A>T
ENST00000473496.1:n.102+27A>T
NM_000771.3:c.331+27A>T NP_000762.2:n.331+27A>T
NM_000771.4:c.331+27A>T MANE Select NP_000762.2:n.331+27A>T
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