Canonical Allele Identifier: CA2610266839
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989054_94989056del , CM000672.2:g.94989054_94989056del GRCh38
NC_000010.10:g.96748811_96748813del , CM000672.1:g.96748811_96748813del GRCh37
NC_000010.9:g.96738801_96738803del NCBI36
NG_008385.1:g.55397_55399del
NG_008385.2:g.55897_55899del

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*26_*28del MANE Select ENSP00000260682.6:n.*26_*28del
ENST00000643112.1:c.*508_*510del ENSP00000496202.1:n.*508_*510del
ENST00000260682.6:c.*26_*28del ENSP00000260682.6:n.*26_*28del
NM_000771.3:c.*26_*28del NP_000762.2:n.*26_*28del
NM_000771.4:c.*26_*28del MANE Select NP_000762.2:n.*26_*28del