Canonical Allele Identifier: CA3428728

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138377833C>T , CM000667.2:g.138377833C>T	GRCh38
NC_000005.9:g.137713522C>T , CM000667.1:g.137713522C>T	GRCh37
NC_000005.8:g.137741421C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.580+8C>T MANE Select	NP_057688.3:n.580+8C>T
ENST00000314358.10:c.580+8C>T MANE Select	ENSP00000326563.5:n.580+8C>T
NM_016604.3:c.580+8C>T	NP_057688.2:n.580+8C>T
ENST00000314358.9:c.580+8C>T	ENSP00000326563.5:n.580+8C>T
ENST00000510866.5:c.388+8C>T	ENSP00000425186.1:n.388+8C>T
ENST00000512928.1:n.269+8C>T
ENST00000542866.2:c.-103+8C>T	ENSP00000439462.2:n.-103+8C>T
XM_005272018.3:c.580+8C>T	XP_005272075.1:n.580+8C>T
XM_005272018.4:c.580+8C>T	XP_005272075.1:n.580+8C>T
XM_011543488.1:c.448+8C>T	XP_011541790.1:n.448+8C>T
XM_011543488.2:c.448+8C>T	XP_011541790.1:n.448+8C>T
XM_011543489.1:c.436+8C>T	XP_011541791.1:n.436+8C>T
XM_011543489.2:c.436+8C>T	XP_011541791.1:n.436+8C>T
XM_024446115.1:c.106+8C>T	XP_024301883.1:n.106+8C>T