Canonical Allele Identifier: CA361094202

Gene: KDM3B

Linked Data

• MyVariant Identifiers: chr5:g.137763700C>T (hg19) ; chr5:g.138428011C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138428011C>T , CM000667.2:g.138428011C>T	GRCh38
NC_000005.9:g.137763700C>T , CM000667.1:g.137763700C>T	GRCh37
NC_000005.8:g.137791599C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000314358.10:c.4678C>T MANE Select	ENSP00000326563.5:p.His1560Tyr
ENST00000314358.9:c.4678C>T	ENSP00000326563.5:p.His1560Tyr
ENST00000507996.5:c.2094C>T	ENSP00000423012.1:n.2094C>T
ENST00000509468.1:n.501C>T
ENST00000510866.5:c.4388C>T	ENSP00000425186.1:n.4388C>T
ENST00000542866.2:c.1672C>T	ENSP00000439462.2:p.His558Tyr
NM_016604.3:c.4678C>T	NP_057688.2:p.His1560Tyr
XM_005272018.3:c.4078C>T	XP_005272075.1:p.His1360Tyr
XM_011543488.1:c.4546C>T	XP_011541790.1:p.His1516Tyr
XM_011543489.1:c.4534C>T	XP_011541791.1:p.His1512Tyr
XM_005272018.4:c.4078C>T	XP_005272075.1:p.His1360Tyr
XM_011543488.2:c.4546C>T	XP_011541790.1:p.His1516Tyr
XM_011543489.2:c.4534C>T	XP_011541791.1:p.His1512Tyr
XM_017009584.1:c.3931C>T	XP_016865073.1:p.His1311Tyr
XM_024446115.1:c.4204C>T	XP_024301883.1:p.His1402Tyr
NM_016604.4:c.4678C>T MANE Select	NP_057688.3:p.His1560Tyr