Canonical Allele Identifier: CA1929349283
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988716A= , CM000672.2:g.94988716A= GRCh38
NC_000010.10:g.96748473A= , CM000672.1:g.96748473A= GRCh37
NC_000010.9:g.96738463A= NCBI36
NG_008385.1:g.55059A=
NG_008385.2:g.55559A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-131A= MANE Select ENSP00000260682.6:n.1292-131A=
ENST00000643112.1:c.*301-131A= ENSP00000496202.1:n.*301-131A=
ENST00000260682.6:c.1292-131A= ENSP00000260682.6:n.1292-131A=
NM_000771.3:c.1292-131A= NP_000762.2:n.1292-131A=
NM_000771.4:c.1292-131A= MANE Select NP_000762.2:n.1292-131A=