Canonical Allele Identifier: CA1929292119
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941771A= , CM000672.2:g.94941771A= GRCh38
NC_000010.10:g.96701528A= , CM000672.1:g.96701528A= GRCh37
NC_000010.9:g.96691518A= NCBI36
NG_008385.1:g.8114A=
NG_008385.2:g.8614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-87A= MANE Select ENSP00000260682.6:n.169-87A=
ENST00000643112.1:c.169-87A= ENSP00000496202.1:n.169-87A=
ENST00000645207.1:n.235A=
ENST00000260682.6:c.169-87A= ENSP00000260682.6:n.169-87A=
ENST00000461906.1:n.194-87A=
NM_000771.3:c.169-87A= NP_000762.2:n.169-87A=
NM_000771.4:c.169-87A= MANE Select NP_000762.2:n.169-87A=
Search 100 bp 5'
Search 100 bp 3'