Canonical Allele Identifier: CA2610268371
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947664del , CM000672.2:g.94947664del GRCh38
NC_000010.10:g.96707421del , CM000672.1:g.96707421del GRCh37
NC_000010.9:g.96697411del NCBI36
NG_008385.1:g.14007del
NG_008385.2:g.14507del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.482-115del MANE Select ENSP00000260682.6:n.482-115del
ENST00000643112.1:c.482-115del ENSP00000496202.1:n.482-115del
ENST00000645207.1:n.635-115del
ENST00000260682.6:c.482-115del ENSP00000260682.6:n.482-115del
ENST00000473496.1:n.253-115del
NM_000771.3:c.482-115del NP_000762.2:n.482-115del
NM_000771.4:c.482-115del MANE Select NP_000762.2:n.482-115del