Canonical Allele Identifier: CA377673942
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949108A>T , CM000672.2:g.94949108A>T GRCh38
NC_000010.10:g.96708865A>T , CM000672.1:g.96708865A>T GRCh37
NC_000010.9:g.96698855A>T NCBI36
NG_008385.1:g.15451A>T
NG_008385.2:g.15951A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643A>T MANE Select ENSP00000260682.6:p.Ile215Phe
ENST00000643112.1:c.643A>T ENSP00000496202.1:p.Ile215Phe
ENST00000260682.6:c.643A>T ENSP00000260682.6:p.Ile215Phe
ENST00000473496.1:n.414A>T
NM_000771.3:c.643A>T NP_000762.2:p.Ile215Phe
NM_000771.4:c.643A>T MANE Select NP_000762.2:p.Ile215Phe