Canonical Allele Identifier: CA5616967
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs371055887

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941897G>C , CM000672.2:g.94941897G>C GRCh38
NC_000010.10:g.96701654G>C , CM000672.1:g.96701654G>C GRCh37
NC_000010.9:g.96691644G>C NCBI36
NG_008385.1:g.8240G>C
NG_008385.2:g.8740G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.208G>C MANE Select ENSP00000260682.6:p.Gly70Arg
ENST00000643112.1:c.208G>C ENSP00000496202.1:p.Gly70Arg
ENST00000645207.1:n.361G>C
ENST00000260682.6:c.208G>C ENSP00000260682.6:p.Gly70Arg
ENST00000461906.1:n.233G>C
NM_000771.3:c.208G>C NP_000762.2:p.Gly70Arg
NM_000771.4:c.208G>C MANE Select NP_000762.2:p.Gly70Arg