Canonical Allele Identifier: CA211694095
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs542021624
gnomAD v3: 10-94942721-G-A
gnomAD v4: 10-94942721-G-A
MyVariant Identifiers: chr10:g.96702478G>A (hg19) chr10:g.94942721G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942721G>A , CM000672.2:g.94942721G>A GRCh38
NC_000010.10:g.96702478G>A , CM000672.1:g.96702478G>A GRCh37
NC_000010.9:g.96692468G>A NCBI36
NG_008385.1:g.9064G>A
NG_008385.2:g.9564G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+380G>A MANE Select ENSP00000260682.6:n.481+380G>A
ENST00000643112.1:c.481+380G>A ENSP00000496202.1:n.481+380G>A
ENST00000645207.1:n.634+380G>A
ENST00000260682.6:c.481+380G>A ENSP00000260682.6:n.481+380G>A
ENST00000461906.1:n.886G>A
ENST00000473496.1:n.252+380G>A
NM_000771.3:c.481+380G>A NP_000762.2:n.481+380G>A
NM_000771.4:c.481+380G>A MANE Select NP_000762.2:n.481+380G>A
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