Canonical Allele Identifier: CA2574622616
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989102C>T , CM000672.2:g.94989102C>T GRCh38
NC_000010.10:g.96748859C>T , CM000672.1:g.96748859C>T GRCh37
NC_000010.9:g.96738849C>T NCBI36
NG_008385.1:g.55445C>T
NG_008385.2:g.55945C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*74C>T MANE Select ENSP00000260682.6:n.*74C>T
ENST00000643112.1:c.*556C>T ENSP00000496202.1:n.*556C>T
ENST00000260682.6:c.*74C>T ENSP00000260682.6:n.*74C>T
NM_000771.3:c.*74C>T NP_000762.2:n.*74C>T
NM_000771.4:c.*74C>T MANE Select NP_000762.2:n.*74C>T