Canonical Allele Identifier: CA2610266458
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981160del , CM000672.2:g.94981160del GRCh38
NC_000010.10:g.96740917del , CM000672.1:g.96740917del GRCh37
NC_000010.9:g.96730907del NCBI36
NG_008385.1:g.47503del
NG_008385.2:g.48003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-23del MANE Select ENSP00000260682.6:n.962-23del
ENST00000643112.1:c.820-23del ENSP00000496202.1:n.820-23del
ENST00000260682.6:c.962-23del ENSP00000260682.6:n.962-23del
NM_000771.3:c.962-23del NP_000762.2:n.962-23del
NM_000771.4:c.962-23del MANE Select NP_000762.2:n.962-23del