Canonical Allele Identifier: CA361094266

Gene: KDM3B

Linked Data

• MyVariant Identifiers: chr5:g.137763713C>G (hg19) ; chr5:g.138428024C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138428024C>G , CM000667.2:g.138428024C>G	GRCh38
NC_000005.9:g.137763713C>G , CM000667.1:g.137763713C>G	GRCh37
NC_000005.8:g.137791612C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000314358.10:c.4691C>G MANE Select	ENSP00000326563.5:p.Ser1564Cys
ENST00000314358.9:c.4691C>G	ENSP00000326563.5:p.Ser1564Cys
ENST00000507996.5:c.2107C>G	ENSP00000423012.1:n.2107C>G
ENST00000509468.1:n.514C>G
ENST00000510866.5:c.4401C>G	ENSP00000425186.1:n.4401C>G
ENST00000542866.2:c.1685C>G	ENSP00000439462.2:p.Ser562Cys
NM_016604.3:c.4691C>G	NP_057688.2:p.Ser1564Cys
XM_005272018.3:c.4091C>G	XP_005272075.1:p.Ser1364Cys
XM_011543488.1:c.4559C>G	XP_011541790.1:p.Ser1520Cys
XM_011543489.1:c.4547C>G	XP_011541791.1:p.Ser1516Cys
XM_005272018.4:c.4091C>G	XP_005272075.1:p.Ser1364Cys
XM_011543488.2:c.4559C>G	XP_011541790.1:p.Ser1520Cys
XM_011543489.2:c.4547C>G	XP_011541791.1:p.Ser1516Cys
XM_017009584.1:c.3944C>G	XP_016865073.1:p.Ser1315Cys
XM_024446115.1:c.4217C>G	XP_024301883.1:p.Ser1406Cys
NM_016604.4:c.4691C>G MANE Select	NP_057688.3:p.Ser1564Cys