Canonical Allele Identifier: CA361108773

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138391794G>A , CM000667.2:g.138391794G>A	GRCh38
NC_000005.9:g.137727483G>A , CM000667.1:g.137727483G>A	GRCh37
NC_000005.8:g.137755382G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.2162G>A MANE Select	ENSP00000326563.5:p.Gly721Glu
ENST00000314358.9:c.2162G>A	ENSP00000326563.5:p.Gly721Glu
ENST00000507996.5:c.46-1377G>A	ENSP00000423012.1:n.46-1377G>A
ENST00000510866.5:c.1872G>A	ENSP00000425186.1:n.1872G>A
ENST00000542866.2:c.-6-6553G>A	ENSP00000439462.2:n.-6-6553G>A
NM_016604.3:c.2162G>A	NP_057688.2:p.Gly721Glu
XM_005272018.3:c.1562G>A	XP_005272075.1:p.Gly521Glu
XM_011543488.1:c.2030G>A	XP_011541790.1:p.Gly677Glu
XM_011543489.1:c.2018G>A	XP_011541791.1:p.Gly673Glu
XM_005272018.4:c.1562G>A	XP_005272075.1:p.Gly521Glu
XM_011543488.2:c.2030G>A	XP_011541790.1:p.Gly677Glu
XM_011543489.2:c.2018G>A	XP_011541791.1:p.Gly673Glu
XM_017009584.1:c.1415G>A	XP_016865073.1:p.Gly472Glu
XM_024446115.1:c.1688G>A	XP_024301883.1:p.Gly563Glu
NM_016604.4:c.2162G>A MANE Select	NP_057688.3:p.Gly721Glu