Canonical Allele Identifier: CA377676168
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981205A>T , CM000672.2:g.94981205A>T GRCh38
NC_000010.10:g.96740962A>T , CM000672.1:g.96740962A>T GRCh37
NC_000010.9:g.96730952A>T NCBI36
NG_008385.1:g.47548A>T
NG_008385.2:g.48048A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.984A>T MANE Select ENSP00000260682.6:p.Glu328Asp
ENST00000643112.1:c.842A>T ENSP00000496202.1:p.Asn281Ile
ENST00000260682.6:c.984A>T ENSP00000260682.6:p.Glu328Asp
NM_000771.3:c.984A>T NP_000762.2:p.Glu328Asp
NM_000771.4:c.984A>T MANE Select NP_000762.2:p.Glu328Asp