Canonical Allele Identifier: CA1929349873
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989089A= , CM000672.2:g.94989089A= GRCh38
NC_000010.10:g.96748846A= , CM000672.1:g.96748846A= GRCh37
NC_000010.9:g.96738836A= NCBI36
NG_008385.1:g.55432A=
NG_008385.2:g.55932A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*61A= MANE Select ENSP00000260682.6:n.*61A=
ENST00000643112.1:c.*543A= ENSP00000496202.1:n.*543A=
ENST00000260682.6:c.*61A= ENSP00000260682.6:n.*61A=
NM_000771.3:c.*61A= NP_000762.2:n.*61A=
NM_000771.4:c.*61A= MANE Select NP_000762.2:n.*61A=