Canonical Allele Identifier: CA361107273

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138391493C>A , CM000667.2:g.138391493C>A	GRCh38
NC_000005.9:g.137727182C>A , CM000667.1:g.137727182C>A	GRCh37
NC_000005.8:g.137755081C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.1861C>A MANE Select	NP_057688.3:p.Leu621Ile
ENST00000314358.10:c.1861C>A MANE Select	ENSP00000326563.5:p.Leu621Ile
NM_016604.3:c.1861C>A	NP_057688.2:p.Leu621Ile
ENST00000314358.9:c.1861C>A	ENSP00000326563.5:p.Leu621Ile
ENST00000507996.5:c.46-1678C>A	ENSP00000423012.1:n.46-1678C>A
ENST00000510866.5:c.1571C>A	ENSP00000425186.1:n.1571C>A
ENST00000542866.2:c.-6-6854C>A	ENSP00000439462.2:n.-6-6854C>A
XM_005272018.3:c.1261C>A	XP_005272075.1:p.Leu421Ile
XM_005272018.4:c.1261C>A	XP_005272075.1:p.Leu421Ile
XM_011543488.1:c.1729C>A	XP_011541790.1:p.Leu577Ile
XM_011543488.2:c.1729C>A	XP_011541790.1:p.Leu577Ile
XM_011543489.1:c.1717C>A	XP_011541791.1:p.Leu573Ile
XM_011543489.2:c.1717C>A	XP_011541791.1:p.Leu573Ile
XM_017009584.1:c.1114C>A	XP_016865073.1:p.Leu372Ile
XM_024446115.1:c.1387C>A	XP_024301883.1:p.Leu463Ile