Canonical Allele Identifier: CA361092916

Gene: KDM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138425520A>G , CM000667.2:g.138425520A>G	GRCh38
NC_000005.9:g.137761209A>G , CM000667.1:g.137761209A>G	GRCh37
NC_000005.8:g.137789108A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016604.4:c.4349A>G MANE Select	NP_057688.3:p.Asn1450Ser
ENST00000314358.10:c.4349A>G MANE Select	ENSP00000326563.5:p.Asn1450Ser
NM_016604.3:c.4349A>G	NP_057688.2:p.Asn1450Ser
ENST00000314358.9:c.4349A>G	ENSP00000326563.5:p.Asn1450Ser
ENST00000505756.1:n.317A>G
ENST00000507996.5:c.1765A>G	ENSP00000423012.1:n.1765A>G
ENST00000510866.5:c.4059A>G	ENSP00000425186.1:n.4059A>G
ENST00000542866.2:c.1343A>G	ENSP00000439462.2:p.Asn448Ser
XM_005272018.3:c.3749A>G	XP_005272075.1:p.Asn1250Ser
XM_005272018.4:c.3749A>G	XP_005272075.1:p.Asn1250Ser
XM_011543488.1:c.4217A>G	XP_011541790.1:p.Asn1406Ser
XM_011543488.2:c.4217A>G	XP_011541790.1:p.Asn1406Ser
XM_011543489.1:c.4205A>G	XP_011541791.1:p.Asn1402Ser
XM_011543489.2:c.4205A>G	XP_011541791.1:p.Asn1402Ser
XM_017009584.1:c.3602A>G	XP_016865073.1:p.Asn1201Ser
XM_024446115.1:c.3875A>G	XP_024301883.1:p.Asn1292Ser