Canonical Allele Identifier: CA1929341845
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981157A= , CM000672.2:g.94981157A= GRCh38
NC_000010.10:g.96740914A= , CM000672.1:g.96740914A= GRCh37
NC_000010.9:g.96730904A= NCBI36
NG_008385.1:g.47500A=
NG_008385.2:g.48000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-26A= MANE Select ENSP00000260682.6:n.962-26A=
ENST00000643112.1:c.820-26A= ENSP00000496202.1:n.820-26A=
ENST00000260682.6:c.962-26A= ENSP00000260682.6:n.962-26A=
NM_000771.3:c.962-26A= NP_000762.2:n.962-26A=
NM_000771.4:c.962-26A= MANE Select NP_000762.2:n.962-26A=