Canonical Allele Identifier: CA377677019
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988932A>T , CM000672.2:g.94988932A>T GRCh38
NC_000010.10:g.96748689A>T , CM000672.1:g.96748689A>T GRCh37
NC_000010.9:g.96738679A>T NCBI36
NG_008385.1:g.55275A>T
NG_008385.2:g.55775A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1377A>T MANE Select ENSP00000260682.6:p.Lys459Asn
ENST00000643112.1:c.*386A>T ENSP00000496202.1:n.*386A>T
ENST00000260682.6:c.1377A>T ENSP00000260682.6:p.Lys459Asn
NM_000771.3:c.1377A>T NP_000762.2:p.Lys459Asn
NM_000771.4:c.1377A>T MANE Select NP_000762.2:p.Lys459Asn