Canonical Allele Identifier: CA403503629

Gene: KDM4B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5137298G>A , CM000681.2:g.5137298G>A	GRCh38
NC_000019.9:g.5137309G>A , CM000681.1:g.5137309G>A	GRCh37
NC_000019.8:g.5088309G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000159111.9:c.2345G>A MANE Select	ENSP00000159111.3:p.Gly782Asp
ENST00000159111.8:c.2345G>A	ENSP00000159111.3:p.Gly782Asp
ENST00000536461.5:c.2447G>A	ENSP00000440495.1:p.Gly816Asp
ENST00000588166.1:n.63G>A
ENST00000588361.1:c.1582G>A
ENST00000589104.5:n.2111G>A
ENST00000611640.4:c.2447G>A	ENSP00000480642.1:p.Gly816Asp
NM_015015.2:c.2345G>A	NP_055830.1:p.Gly782Asp
XM_005259521.2:c.2447G>A	XP_005259578.2:p.Gly816Asp
XM_005259522.3:c.1352G>A	XP_005259579.2:p.Gly451Asp
XM_011527814.1:c.2171G>A	XP_011526116.1:p.Gly724Asp
XM_011527815.1:c.2447G>A	XP_011526117.1:p.Gly816Asp
XM_011527816.1:c.1418G>A	XP_011526118.1:p.Gly473Asp
XM_011527817.1:c.1367G>A	XP_011526119.1:p.Gly456Asp
XM_005259521.4:c.2447G>A	XP_005259578.2:p.Gly816Asp
XM_011527814.2:c.2171G>A	XP_011526116.1:p.Gly724Asp
XM_011527816.2:c.1418G>A	XP_011526118.1:p.Gly473Asp
XM_011527817.2:c.1367G>A	XP_011526119.1:p.Gly456Asp
XM_017026503.1:c.2447G>A	XP_016881992.1:p.Gly816Asp
NM_015015.3:c.2345G>A MANE Select	NP_055830.1:p.Gly782Asp