Canonical Allele Identifier: CA1929335163
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974643G= , CM000672.2:g.94974643G= GRCh38
NC_000010.10:g.96734400G= , CM000672.1:g.96734400G= GRCh37
NC_000010.9:g.96724390G= NCBI36
NG_008385.1:g.40986G=
NG_008385.2:g.41486G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2398G= MANE Select ENSP00000260682.6:n.961+2398G=
ENST00000643112.1:c.820-6540G= ENSP00000496202.1:n.820-6540G=
ENST00000260682.6:c.961+2398G= ENSP00000260682.6:n.961+2398G=
NM_000771.3:c.961+2398G= NP_000762.2:n.961+2398G=
NM_000771.4:c.961+2398G= MANE Select NP_000762.2:n.961+2398G=
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