Canonical Allele Identifier: CA361090172

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138420888G>C , CM000667.2:g.138420888G>C	GRCh38
NC_000005.9:g.137756577G>C , CM000667.1:g.137756577G>C	GRCh37
NC_000005.8:g.137784476G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.3898G>C MANE Select	NP_057688.3:p.Gly1300Arg
ENST00000314358.10:c.3898G>C MANE Select	ENSP00000326563.5:p.Gly1300Arg
NM_016604.3:c.3898G>C	NP_057688.2:p.Gly1300Arg
ENST00000314358.9:c.3898G>C	ENSP00000326563.5:p.Gly1300Arg
ENST00000507996.5:c.1314G>C	ENSP00000423012.1:n.1314G>C
ENST00000510866.5:c.3608G>C	ENSP00000425186.1:n.3608G>C
ENST00000542866.2:c.892G>C	ENSP00000439462.2:p.Gly298Arg
XM_005272018.3:c.3298G>C	XP_005272075.1:p.Gly1100Arg
XM_005272018.4:c.3298G>C	XP_005272075.1:p.Gly1100Arg
XM_011543488.1:c.3766G>C	XP_011541790.1:p.Gly1256Arg
XM_011543488.2:c.3766G>C	XP_011541790.1:p.Gly1256Arg
XM_011543489.1:c.3754G>C	XP_011541791.1:p.Gly1252Arg
XM_011543489.2:c.3754G>C	XP_011541791.1:p.Gly1252Arg
XM_017009584.1:c.3151G>C	XP_016865073.1:p.Gly1051Arg
XM_024446115.1:c.3424G>C	XP_024301883.1:p.Gly1142Arg