Canonical Allele Identifier: CA5616999
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs755877934

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941999G>T , CM000672.2:g.94941999G>T GRCh38
NC_000010.10:g.96701756G>T , CM000672.1:g.96701756G>T GRCh37
NC_000010.9:g.96691746G>T NCBI36
NG_008385.1:g.8342G>T
NG_008385.2:g.8842G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.310G>T MANE Select ENSP00000260682.6:p.Glu104Ter
ENST00000643112.1:c.310G>T ENSP00000496202.1:p.Glu104Ter
ENST00000645207.1:n.463G>T
ENST00000260682.6:c.310G>T ENSP00000260682.6:p.Glu104Ter
ENST00000461906.1:n.335G>T
ENST00000473496.1:n.81G>T
NM_000771.3:c.310G>T NP_000762.2:p.Glu104Ter
NM_000771.4:c.310G>T MANE Select NP_000762.2:p.Glu104Ter