Canonical Allele Identifier: CA1929292661
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942714C= , CM000672.2:g.94942714C= GRCh38
NC_000010.10:g.96702471C= , CM000672.1:g.96702471C= GRCh37
NC_000010.9:g.96692461C= NCBI36
NG_008385.1:g.9057C=
NG_008385.2:g.9557C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+373C= MANE Select ENSP00000260682.6:n.481+373C=
ENST00000643112.1:c.481+373C= ENSP00000496202.1:n.481+373C=
ENST00000645207.1:n.634+373C=
ENST00000260682.6:c.481+373C= ENSP00000260682.6:n.481+373C=
ENST00000461906.1:n.879C=
ENST00000473496.1:n.252+373C=
NM_000771.3:c.481+373C= NP_000762.2:n.481+373C=
NM_000771.4:c.481+373C= MANE Select NP_000762.2:n.481+373C=
Search 100 bp 5'
Search 100 bp 3'