Canonical Allele Identifier: CA670178724
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1349094224

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974668dup , CM000672.2:g.94974668dup GRCh38
NC_000010.10:g.96734425dup , CM000672.1:g.96734425dup GRCh37
NC_000010.9:g.96724415dup NCBI36
NG_008385.1:g.41011dup
NG_008385.2:g.41511dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2423dup MANE Select ENSP00000260682.6:n.961+2423dup
ENST00000643112.1:c.820-6515dup ENSP00000496202.1:n.820-6515dup
ENST00000260682.6:c.961+2423dup ENSP00000260682.6:n.961+2423dup
NM_000771.3:c.961+2423dup NP_000762.2:n.961+2423dup
NM_000771.4:c.961+2423dup MANE Select NP_000762.2:n.961+2423dup