Canonical Allele Identifier: CA1929292406
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942218T= , CM000672.2:g.94942218T= GRCh38
NC_000010.10:g.96701975T= , CM000672.1:g.96701975T= GRCh37
NC_000010.9:g.96691965T= NCBI36
NG_008385.1:g.8561T=
NG_008385.2:g.9061T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.358T= MANE Select ENSP00000260682.6:p.Trp120=
ENST00000643112.1:c.358T= ENSP00000496202.1:p.Trp120=
ENST00000645207.1:n.511T=
ENST00000260682.6:c.358T= ENSP00000260682.6:p.Trp120=
ENST00000461906.1:n.383T=
ENST00000473496.1:n.129T=
NM_000771.3:c.358T= NP_000762.2:p.Trp120=
NM_000771.4:c.358T= MANE Select NP_000762.2:p.Trp120=