Canonical Allele Identifier: CA1929292282
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031396207
gnomAD v4: 10-94942048-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942048T>A , CM000672.2:g.94942048T>A GRCh38
NC_000010.10:g.96701805T>A , CM000672.1:g.96701805T>A GRCh37
NC_000010.9:g.96691795T>A NCBI36
NG_008385.1:g.8391T>A
NG_008385.2:g.8891T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+28T>A MANE Select ENSP00000260682.6:n.331+28T>A
ENST00000643112.1:c.331+28T>A ENSP00000496202.1:n.331+28T>A
ENST00000645207.1:n.484+28T>A
ENST00000260682.6:c.331+28T>A ENSP00000260682.6:n.331+28T>A
ENST00000461906.1:n.356+28T>A
ENST00000473496.1:n.102+28T>A
NM_000771.3:c.331+28T>A NP_000762.2:n.331+28T>A
NM_000771.4:c.331+28T>A MANE Select NP_000762.2:n.331+28T>A
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