Canonical Allele Identifier: CA1929292316
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942095C= , CM000672.2:g.94942095C= GRCh38
NC_000010.10:g.96701852C= , CM000672.1:g.96701852C= GRCh37
NC_000010.9:g.96691842C= NCBI36
NG_008385.1:g.8438C=
NG_008385.2:g.8938C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+75C= MANE Select ENSP00000260682.6:n.331+75C=
ENST00000643112.1:c.331+75C= ENSP00000496202.1:n.331+75C=
ENST00000645207.1:n.484+75C=
ENST00000260682.6:c.331+75C= ENSP00000260682.6:n.331+75C=
ENST00000461906.1:n.356+75C=
ENST00000473496.1:n.102+75C=
NM_000771.3:c.331+75C= NP_000762.2:n.331+75C=
NM_000771.4:c.331+75C= MANE Select NP_000762.2:n.331+75C=