Canonical Allele Identifier: CA1929296050
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947309C= , CM000672.2:g.94947309C= GRCh38
NC_000010.10:g.96707066C= , CM000672.1:g.96707066C= GRCh37
NC_000010.9:g.96697056C= NCBI36
NG_008385.1:g.13652C=
NG_008385.2:g.14152C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.482-470C= MANE Select ENSP00000260682.6:n.482-470C=
ENST00000643112.1:c.482-470C= ENSP00000496202.1:n.482-470C=
ENST00000645207.1:n.635-470C=
ENST00000260682.6:c.482-470C= ENSP00000260682.6:n.482-470C=
ENST00000473496.1:n.253-470C=
NM_000771.3:c.482-470C= NP_000762.2:n.482-470C=
NM_000771.4:c.482-470C= MANE Select NP_000762.2:n.482-470C=
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