Canonical Allele Identifier: CA1585838051

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138428109C= , CM000667.2:g.138428109C=	GRCh38
NC_000005.9:g.137763798C= , CM000667.1:g.137763798C=	GRCh37
NC_000005.8:g.137791697C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.4753+23C= MANE Select	NP_057688.3:n.4753+23C=
ENST00000314358.10:c.4753+23C= MANE Select	ENSP00000326563.5:n.4753+23C=
NM_016604.3:c.4753+23C=	NP_057688.2:n.4753+23C=
ENST00000314358.9:c.4753+23C=	ENSP00000326563.5:n.4753+23C=
ENST00000507996.5:c.2169+23C=	ENSP00000423012.1:n.2169+23C=
ENST00000510866.5:c.4463+23C=	ENSP00000425186.1:n.4463+23C=
ENST00000542866.2:c.1747+23C=	ENSP00000439462.2:n.1747+23C=
XM_005272018.3:c.4153+23C=	XP_005272075.1:n.4153+23C=
XM_005272018.4:c.4153+23C=	XP_005272075.1:n.4153+23C=
XM_011543488.1:c.4621+23C=	XP_011541790.1:n.4621+23C=
XM_011543488.2:c.4621+23C=	XP_011541790.1:n.4621+23C=
XM_011543489.1:c.4609+23C=	XP_011541791.1:n.4609+23C=
XM_011543489.2:c.4609+23C=	XP_011541791.1:n.4609+23C=
XM_017009584.1:c.4006+23C=	XP_016865073.1:n.4006+23C=
XM_024446115.1:c.4279+23C=	XP_024301883.1:n.4279+23C=