Canonical Allele Identifier: CA3429064

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138392174A>G , CM000667.2:g.138392174A>G	GRCh38
NC_000005.9:g.137727863A>G , CM000667.1:g.137727863A>G	GRCh37
NC_000005.8:g.137755762A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.2542A>G MANE Select	ENSP00000326563.5:p.Asn848Asp
ENST00000314358.9:c.2542A>G	ENSP00000326563.5:p.Asn848Asp
ENST00000507996.5:c.46-997A>G	ENSP00000423012.1:n.46-997A>G
ENST00000510866.5:c.2252A>G	ENSP00000425186.1:n.2252A>G
ENST00000542866.2:c.-6-6173A>G	ENSP00000439462.2:n.-6-6173A>G
NM_016604.3:c.2542A>G	NP_057688.2:p.Asn848Asp
XM_005272018.3:c.1942A>G	XP_005272075.1:p.Asn648Asp
XM_011543488.1:c.2410A>G	XP_011541790.1:p.Asn804Asp
XM_011543489.1:c.2398A>G	XP_011541791.1:p.Asn800Asp
XM_005272018.4:c.1942A>G	XP_005272075.1:p.Asn648Asp
XM_011543488.2:c.2410A>G	XP_011541790.1:p.Asn804Asp
XM_011543489.2:c.2398A>G	XP_011541791.1:p.Asn800Asp
XM_017009584.1:c.1795A>G	XP_016865073.1:p.Asn599Asp
XM_024446115.1:c.2068A>G	XP_024301883.1:p.Asn690Asp
NM_016604.4:c.2542A>G MANE Select	NP_057688.3:p.Asn848Asp