Canonical Allele Identifier: CA1929292617
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942619A= , CM000672.2:g.94942619A= GRCh38
NC_000010.10:g.96702376A= , CM000672.1:g.96702376A= GRCh37
NC_000010.9:g.96692366A= NCBI36
NG_008385.1:g.8962A=
NG_008385.2:g.9462A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+278A= MANE Select ENSP00000260682.6:n.481+278A=
ENST00000643112.1:c.481+278A= ENSP00000496202.1:n.481+278A=
ENST00000645207.1:n.634+278A=
ENST00000260682.6:c.481+278A= ENSP00000260682.6:n.481+278A=
ENST00000461906.1:n.784A=
ENST00000473496.1:n.252+278A=
NM_000771.3:c.481+278A= NP_000762.2:n.481+278A=
NM_000771.4:c.481+278A= MANE Select NP_000762.2:n.481+278A=
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