Canonical Allele Identifier: CA3429437

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138425569C>T , CM000667.2:g.138425569C>T	GRCh38
NC_000005.9:g.137761258C>T , CM000667.1:g.137761258C>T	GRCh37
NC_000005.8:g.137789157C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.4398C>T MANE Select	ENSP00000326563.5:p.Phe1466=
ENST00000314358.9:c.4398C>T	ENSP00000326563.5:p.Phe1466=
ENST00000505756.1:n.366C>T
ENST00000507996.5:c.1814C>T	ENSP00000423012.1:n.1814C>T
ENST00000510866.5:c.4108C>T	ENSP00000425186.1:n.4108C>T
ENST00000542866.2:c.1392C>T	ENSP00000439462.2:p.Phe464=
NM_016604.3:c.4398C>T	NP_057688.2:p.Phe1466=
XM_005272018.3:c.3798C>T	XP_005272075.1:p.Phe1266=
XM_011543488.1:c.4266C>T	XP_011541790.1:p.Phe1422=
XM_011543489.1:c.4254C>T	XP_011541791.1:p.Phe1418=
XM_005272018.4:c.3798C>T	XP_005272075.1:p.Phe1266=
XM_011543488.2:c.4266C>T	XP_011541790.1:p.Phe1422=
XM_011543489.2:c.4254C>T	XP_011541791.1:p.Phe1418=
XM_017009584.1:c.3651C>T	XP_016865073.1:p.Phe1217=
XM_024446115.1:c.3924C>T	XP_024301883.1:p.Phe1308=
NM_016604.4:c.4398C>T MANE Select	NP_057688.3:p.Phe1466=