Canonical Allele Identifier: CA1929349451
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988832G= , CM000672.2:g.94988832G= GRCh38
NC_000010.10:g.96748589G= , CM000672.1:g.96748589G= GRCh37
NC_000010.9:g.96738579G= NCBI36
NG_008385.1:g.55175G=
NG_008385.2:g.55675G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1292-15G= MANE Select ENSP00000260682.6:n.1292-15G=
ENST00000643112.1:c.*301-15G= ENSP00000496202.1:n.*301-15G=
ENST00000260682.6:c.1292-15G= ENSP00000260682.6:n.1292-15G=
NM_000771.3:c.1292-15G= NP_000762.2:n.1292-15G=
NM_000771.4:c.1292-15G= MANE Select NP_000762.2:n.1292-15G=