Canonical Allele Identifier: CA2610266791
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94988750-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988750T>A , CM000672.2:g.94988750T>A GRCh38
NC_000010.10:g.96748507T>A , CM000672.1:g.96748507T>A GRCh37
NC_000010.9:g.96738497T>A NCBI36
NG_008385.1:g.55093T>A
NG_008385.2:g.55593T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-97T>A MANE Select ENSP00000260682.6:n.1292-97T>A
ENST00000643112.1:c.*301-97T>A ENSP00000496202.1:n.*301-97T>A
ENST00000260682.6:c.1292-97T>A ENSP00000260682.6:n.1292-97T>A
NM_000771.3:c.1292-97T>A NP_000762.2:n.1292-97T>A
NM_000771.4:c.1292-97T>A MANE Select NP_000762.2:n.1292-97T>A
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