Canonical Allele Identifier: CA361093747

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138427192T>G , CM000667.2:g.138427192T>G	GRCh38
NC_000005.9:g.137762881T>G , CM000667.1:g.137762881T>G	GRCh37
NC_000005.8:g.137790780T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.4506T>G MANE Select	ENSP00000326563.5:p.Phe1502Leu
ENST00000314358.9:c.4506T>G	ENSP00000326563.5:p.Phe1502Leu
ENST00000507996.5:c.1922T>G	ENSP00000423012.1:n.1922T>G
ENST00000509468.1:n.329T>G
ENST00000510866.5:c.4216T>G	ENSP00000425186.1:n.4216T>G
ENST00000542866.2:c.1500T>G	ENSP00000439462.2:p.Phe500Leu
NM_016604.3:c.4506T>G	NP_057688.2:p.Phe1502Leu
XM_005272018.3:c.3906T>G	XP_005272075.1:p.Phe1302Leu
XM_011543488.1:c.4374T>G	XP_011541790.1:p.Phe1458Leu
XM_011543489.1:c.4362T>G	XP_011541791.1:p.Phe1454Leu
XM_005272018.4:c.3906T>G	XP_005272075.1:p.Phe1302Leu
XM_011543488.2:c.4374T>G	XP_011541790.1:p.Phe1458Leu
XM_011543489.2:c.4362T>G	XP_011541791.1:p.Phe1454Leu
XM_017009584.1:c.3759T>G	XP_016865073.1:p.Phe1253Leu
XM_024446115.1:c.4032T>G	XP_024301883.1:p.Phe1344Leu
NM_016604.4:c.4506T>G MANE Select	NP_057688.3:p.Phe1502Leu