Canonical Allele Identifier: CA1929292278
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942045G= , CM000672.2:g.94942045G= GRCh38
NC_000010.10:g.96701802G= , CM000672.1:g.96701802G= GRCh37
NC_000010.9:g.96691792G= NCBI36
NG_008385.1:g.8388G=
NG_008385.2:g.8888G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+25G= MANE Select ENSP00000260682.6:n.331+25G=
ENST00000643112.1:c.331+25G= ENSP00000496202.1:n.331+25G=
ENST00000645207.1:n.484+25G=
ENST00000260682.6:c.331+25G= ENSP00000260682.6:n.331+25G=
ENST00000461906.1:n.356+25G=
ENST00000473496.1:n.102+25G=
NM_000771.3:c.331+25G= NP_000762.2:n.331+25G=
NM_000771.4:c.331+25G= MANE Select NP_000762.2:n.331+25G=
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