Canonical Allele Identifier: CA361094212

Gene: KDM3B

Linked Data

• MyVariant Identifiers: chr5:g.137763702C>A (hg19) ; chr5:g.138428013C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138428013C>A , CM000667.2:g.138428013C>A	GRCh38
NC_000005.9:g.137763702C>A , CM000667.1:g.137763702C>A	GRCh37
NC_000005.8:g.137791601C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000314358.10:c.4680C>A MANE Select	ENSP00000326563.5:p.His1560Gln
ENST00000314358.9:c.4680C>A	ENSP00000326563.5:p.His1560Gln
ENST00000507996.5:c.2096C>A	ENSP00000423012.1:n.2096C>A
ENST00000509468.1:n.503C>A
ENST00000510866.5:c.4390C>A	ENSP00000425186.1:n.4390C>A
ENST00000542866.2:c.1674C>A	ENSP00000439462.2:p.His558Gln
NM_016604.3:c.4680C>A	NP_057688.2:p.His1560Gln
XM_005272018.3:c.4080C>A	XP_005272075.1:p.His1360Gln
XM_011543488.1:c.4548C>A	XP_011541790.1:p.His1516Gln
XM_011543489.1:c.4536C>A	XP_011541791.1:p.His1512Gln
XM_005272018.4:c.4080C>A	XP_005272075.1:p.His1360Gln
XM_011543488.2:c.4548C>A	XP_011541790.1:p.His1516Gln
XM_011543489.2:c.4536C>A	XP_011541791.1:p.His1512Gln
XM_017009584.1:c.3933C>A	XP_016865073.1:p.His1311Gln
XM_024446115.1:c.4206C>A	XP_024301883.1:p.His1402Gln
NM_016604.4:c.4680C>A MANE Select	NP_057688.3:p.His1560Gln