Canonical Allele Identifier: CA3428807

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138386045A>G , CM000667.2:g.138386045A>G	GRCh38
NC_000005.9:g.137721734A>G , CM000667.1:g.137721734A>G	GRCh37
NC_000005.8:g.137749633A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.804A>G MANE Select	ENSP00000326563.5:p.Lys268=
ENST00000314358.9:c.804A>G	ENSP00000326563.5:p.Lys268=
ENST00000510866.5:c.612A>G	ENSP00000425186.1:p.Lys204=
ENST00000542866.2:c.-7+6366A>G	ENSP00000439462.2:n.-7+6366A>G
NM_016604.3:c.804A>G	NP_057688.2:p.Lys268=
XM_005272018.3:c.780+4455A>G	XP_005272075.1:n.780+4455A>G
XM_011543488.1:c.672A>G	XP_011541790.1:p.Lys224=
XM_011543489.1:c.660A>G	XP_011541791.1:p.Lys220=
XM_005272018.4:c.780+4455A>G	XP_005272075.1:n.780+4455A>G
XM_011543488.2:c.672A>G	XP_011541790.1:p.Lys224=
XM_011543489.2:c.660A>G	XP_011541791.1:p.Lys220=
XM_017009584.1:c.57A>G	XP_016865073.1:p.Lys19=
XM_024446115.1:c.330A>G	XP_024301883.1:p.Lys110=
NM_016604.4:c.804A>G MANE Select	NP_057688.3:p.Lys268=