Canonical Allele Identifier: CA2610268370
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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