Canonical Allele Identifier: CA1929292258
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942014G= , CM000672.2:g.94942014G= GRCh38
NC_000010.10:g.96701771G= , CM000672.1:g.96701771G= GRCh37
NC_000010.9:g.96691761G= NCBI36
NG_008385.1:g.8357G=
NG_008385.2:g.8857G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.325G= MANE Select ENSP00000260682.6:p.Gly109=
ENST00000643112.1:c.325G= ENSP00000496202.1:p.Gly109=
ENST00000645207.1:n.478G=
ENST00000260682.6:c.325G= ENSP00000260682.6:p.Gly109=
ENST00000461906.1:n.350G=
ENST00000473496.1:n.96G=
NM_000771.3:c.325G= NP_000762.2:p.Gly109=
NM_000771.4:c.325G= MANE Select NP_000762.2:p.Gly109=