Canonical Allele Identifier: CA1929292080
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941705A= , CM000672.2:g.94941705A= GRCh38
NC_000010.10:g.96701462A= , CM000672.1:g.96701462A= GRCh37
NC_000010.9:g.96691452A= NCBI36
NG_008385.1:g.8048A=
NG_008385.2:g.8548A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-153A= MANE Select ENSP00000260682.6:n.169-153A=
ENST00000643112.1:c.169-153A= ENSP00000496202.1:n.169-153A=
ENST00000645207.1:n.169A=
ENST00000260682.6:c.169-153A= ENSP00000260682.6:n.169-153A=
ENST00000461906.1:n.194-153A=
NM_000771.3:c.169-153A= NP_000762.2:n.169-153A=
NM_000771.4:c.169-153A= MANE Select NP_000762.2:n.169-153A=
Search 100 bp 5'
Search 100 bp 3'