Canonical Allele Identifier: CA377672961
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942190A>C , CM000672.2:g.94942190A>C GRCh38
NC_000010.10:g.96701947A>C , CM000672.1:g.96701947A>C GRCh37
NC_000010.9:g.96691937A>C NCBI36
NG_008385.1:g.8533A>C
NG_008385.2:g.9033A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.332-2A>C MANE Select ENSP00000260682.6:p.=
ENST00000643112.1:c.332-2A>C ENSP00000496202.1:p.=
ENST00000645207.1:n.485-2A>C
ENST00000260682.6:c.332-2A>C ENSP00000260682.6:p.=
ENST00000461906.1:n.357-2A>C
ENST00000473496.1:n.103-2A>C
NM_000771.3:c.332-2A>C NP_000762.2:p.=
NM_000771.4:c.332-2A>C MANE Select NP_000762.2:p.=