Canonical Allele Identifier: CA446595359

Gene: KDM3B

Linked Data

• MyVariant Identifiers: chr5:g.137763711G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138428022G>T , CM000667.2:g.138428022G>T	GRCh38
NC_000005.9:g.137763711G>T , CM000667.1:g.137763711G>T	GRCh37
NC_000005.8:g.137791610G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000314358.10:c.4689G>T MANE Select	ENSP00000326563.5:p.Val1563=
ENST00000314358.9:c.4689G>T	ENSP00000326563.5:p.Val1563=
ENST00000507996.5:c.2105G>T	ENSP00000423012.1:n.2105G>T
ENST00000509468.1:n.512G>T
ENST00000510866.5:c.4399G>T	ENSP00000425186.1:n.4399G>T
ENST00000542866.2:c.1683G>T	ENSP00000439462.2:p.Val561=
NM_016604.3:c.4689G>T	NP_057688.2:p.Val1563=
XM_005272018.3:c.4089G>T	XP_005272075.1:p.Val1363=
XM_011543488.1:c.4557G>T	XP_011541790.1:p.Val1519=
XM_011543489.1:c.4545G>T	XP_011541791.1:p.Val1515=
XM_005272018.4:c.4089G>T	XP_005272075.1:p.Val1363=
XM_011543488.2:c.4557G>T	XP_011541790.1:p.Val1519=
XM_011543489.2:c.4545G>T	XP_011541791.1:p.Val1515=
XM_017009584.1:c.3942G>T	XP_016865073.1:p.Val1314=
XM_024446115.1:c.4215G>T	XP_024301883.1:p.Val1405=
NM_016604.4:c.4689G>T MANE Select	NP_057688.3:p.Val1563=