Canonical Allele Identifier: CA1929292319
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942097C= , CM000672.2:g.94942097C= GRCh38
NC_000010.10:g.96701854C= , CM000672.1:g.96701854C= GRCh37
NC_000010.9:g.96691844C= NCBI36
NG_008385.1:g.8440C=
NG_008385.2:g.8940C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+77C= MANE Select ENSP00000260682.6:n.331+77C=
ENST00000643112.1:c.331+77C= ENSP00000496202.1:n.331+77C=
ENST00000645207.1:n.484+77C=
ENST00000260682.6:c.331+77C= ENSP00000260682.6:n.331+77C=
ENST00000461906.1:n.356+77C=
ENST00000473496.1:n.102+77C=
NM_000771.3:c.331+77C= NP_000762.2:n.331+77C=
NM_000771.4:c.331+77C= MANE Select NP_000762.2:n.331+77C=