Canonical Allele Identifier: CA931385821
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1412962257

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989089A>T , CM000672.2:g.94989089A>T GRCh38
NC_000010.10:g.96748846A>T , CM000672.1:g.96748846A>T GRCh37
NC_000010.9:g.96738836A>T NCBI36
NG_008385.1:g.55432A>T
NG_008385.2:g.55932A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*61A>T MANE Select ENSP00000260682.6:n.*61A>T
ENST00000643112.1:c.*543A>T ENSP00000496202.1:n.*543A>T
ENST00000260682.6:c.*61A>T ENSP00000260682.6:n.*61A>T
NM_000771.3:c.*61A>T NP_000762.2:n.*61A>T
NM_000771.4:c.*61A>T MANE Select NP_000762.2:n.*61A>T