Canonical Allele Identifier: CA1929292128
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941787A= , CM000672.2:g.94941787A= GRCh38
NC_000010.10:g.96701544A= , CM000672.1:g.96701544A= GRCh37
NC_000010.9:g.96691534A= NCBI36
NG_008385.1:g.8130A=
NG_008385.2:g.8630A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-71A= MANE Select ENSP00000260682.6:n.169-71A=
ENST00000643112.1:c.169-71A= ENSP00000496202.1:n.169-71A=
ENST00000645207.1:n.251A=
ENST00000260682.6:c.169-71A= ENSP00000260682.6:n.169-71A=
ENST00000461906.1:n.194-71A=
NM_000771.3:c.169-71A= NP_000762.2:n.169-71A=
NM_000771.4:c.169-71A= MANE Select NP_000762.2:n.169-71A=
Search 100 bp 5'
Search 100 bp 3'