Canonical Allele Identifier: CA1929349305
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988748G= , CM000672.2:g.94988748G= GRCh38
NC_000010.10:g.96748505G= , CM000672.1:g.96748505G= GRCh37
NC_000010.9:g.96738495G= NCBI36
NG_008385.1:g.55091G=
NG_008385.2:g.55591G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-99G= MANE Select ENSP00000260682.6:n.1292-99G=
ENST00000643112.1:c.*301-99G= ENSP00000496202.1:n.*301-99G=
ENST00000260682.6:c.1292-99G= ENSP00000260682.6:n.1292-99G=
NM_000771.3:c.1292-99G= NP_000762.2:n.1292-99G=
NM_000771.4:c.1292-99G= MANE Select NP_000762.2:n.1292-99G=