Canonical Allele Identifier: CA361096992

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138430357G>C , CM000667.2:g.138430357G>C	GRCh38
NC_000005.9:g.137766046G>C , CM000667.1:g.137766046G>C	GRCh37
NC_000005.8:g.137793945G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.5002G>C MANE Select	ENSP00000326563.5:p.Val1668Leu
ENST00000314358.9:c.5002G>C	ENSP00000326563.5:p.Val1668Leu
ENST00000507996.5:c.2418G>C	ENSP00000423012.1:n.2418G>C
ENST00000510866.5:c.4712G>C	ENSP00000425186.1:n.4712G>C
ENST00000542866.2:c.1996G>C	ENSP00000439462.2:p.Val666Leu
NM_016604.3:c.5002G>C	NP_057688.2:p.Val1668Leu
XM_005272018.3:c.4402G>C	XP_005272075.1:p.Val1468Leu
XM_011543488.1:c.4870G>C	XP_011541790.1:p.Val1624Leu
XM_011543489.1:c.4858G>C	XP_011541791.1:p.Val1620Leu
XM_005272018.4:c.4402G>C	XP_005272075.1:p.Val1468Leu
XM_011543488.2:c.4870G>C	XP_011541790.1:p.Val1624Leu
XM_011543489.2:c.4858G>C	XP_011541791.1:p.Val1620Leu
XM_017009584.1:c.4255G>C	XP_016865073.1:p.Val1419Leu
XM_024446115.1:c.4528G>C	XP_024301883.1:p.Val1510Leu
NM_016604.4:c.5002G>C MANE Select	NP_057688.3:p.Val1668Leu