Canonical Allele Identifier: CA361111308

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138393302C>T , CM000667.2:g.138393302C>T	GRCh38
NC_000005.9:g.137728991C>T , CM000667.1:g.137728991C>T	GRCh37
NC_000005.8:g.137756890C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.2761C>T MANE Select	ENSP00000326563.5:p.Arg921Trp
ENST00000314358.9:c.2761C>T	ENSP00000326563.5:p.Arg921Trp
ENST00000507996.5:c.177C>T	ENSP00000423012.1:n.177C>T
ENST00000510866.5:c.2471C>T	ENSP00000425186.1:n.2471C>T
ENST00000542866.2:c.-6-5045C>T	ENSP00000439462.2:n.-6-5045C>T
NM_016604.3:c.2761C>T	NP_057688.2:p.Arg921Trp
XM_005272018.3:c.2161C>T	XP_005272075.1:p.Arg721Trp
XM_011543488.1:c.2629C>T	XP_011541790.1:p.Arg877Trp
XM_011543489.1:c.2617C>T	XP_011541791.1:p.Arg873Trp
XM_005272018.4:c.2161C>T	XP_005272075.1:p.Arg721Trp
XM_011543488.2:c.2629C>T	XP_011541790.1:p.Arg877Trp
XM_011543489.2:c.2617C>T	XP_011541791.1:p.Arg873Trp
XM_017009584.1:c.2014C>T	XP_016865073.1:p.Arg672Trp
XM_024446115.1:c.2287C>T	XP_024301883.1:p.Arg763Trp
NM_016604.4:c.2761C>T MANE Select	NP_057688.3:p.Arg921Trp