Canonical Allele Identifier: CA361080727

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138399859G>A , CM000667.2:g.138399859G>A	GRCh38
NC_000005.9:g.137735548G>A , CM000667.1:g.137735548G>A	GRCh37
NC_000005.8:g.137763447G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.3047-1G>A MANE Select	NP_057688.3:n.3047-1G>A
ENST00000314358.10:c.3047-1G>A MANE Select	ENSP00000326563.5:n.3047-1G>A
NM_016604.3:c.3047-1G>A	NP_057688.2:n.3047-1G>A
ENST00000314358.9:c.3047-1G>A	ENSP00000326563.5:n.3047-1G>A
ENST00000504095.1:n.516-1G>A
ENST00000507996.5:c.463-1G>A	ENSP00000423012.1:n.463-1G>A
ENST00000510866.5:c.2757-1G>A	ENSP00000425186.1:n.2757-1G>A
ENST00000542866.2:c.41-1G>A	ENSP00000439462.2:n.41-1G>A
XM_005272018.3:c.2447-1G>A	XP_005272075.1:n.2447-1G>A
XM_005272018.4:c.2447-1G>A	XP_005272075.1:n.2447-1G>A
XM_011543488.1:c.2915-1G>A	XP_011541790.1:n.2915-1G>A
XM_011543488.2:c.2915-1G>A	XP_011541790.1:n.2915-1G>A
XM_011543489.1:c.2903-1G>A	XP_011541791.1:n.2903-1G>A
XM_011543489.2:c.2903-1G>A	XP_011541791.1:n.2903-1G>A
XM_017009584.1:c.2300-1G>A	XP_016865073.1:n.2300-1G>A
XM_024446115.1:c.2573-1G>A	XP_024301883.1:n.2573-1G>A