Canonical Allele Identifier: CA1929292682
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942748G= , CM000672.2:g.94942748G= GRCh38
NC_000010.10:g.96702505G= , CM000672.1:g.96702505G= GRCh37
NC_000010.9:g.96692495G= NCBI36
NG_008385.1:g.9091G=
NG_008385.2:g.9591G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+407G= MANE Select ENSP00000260682.6:n.481+407G=
ENST00000643112.1:c.481+407G= ENSP00000496202.1:n.481+407G=
ENST00000645207.1:n.634+407G=
ENST00000260682.6:c.481+407G= ENSP00000260682.6:n.481+407G=
ENST00000461906.1:n.913G=
ENST00000473496.1:n.252+407G=
NM_000771.3:c.481+407G= NP_000762.2:n.481+407G=
NM_000771.4:c.481+407G= MANE Select NP_000762.2:n.481+407G=
Search 100 bp 5'
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