Canonical Allele Identifier: CA361093736
Gene: KDM3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.138427190T>C , CM000667.2:g.138427190T>C GRCh38
NC_000005.9:g.137762879T>C , CM000667.1:g.137762879T>C GRCh37
NC_000005.8:g.137790778T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000314358.10:c.4504T>C MANE Select ENSP00000326563.5:p.Phe1502Leu
ENST00000314358.9:c.4504T>C ENSP00000326563.5:p.Phe1502Leu
ENST00000507996.5:c.1920T>C ENSP00000423012.1:n.1920T>C
ENST00000509468.1:n.327T>C
ENST00000510866.5:c.4214T>C ENSP00000425186.1:n.4214T>C
ENST00000542866.2:c.1498T>C ENSP00000439462.2:p.Phe500Leu
NM_016604.3:c.4504T>C NP_057688.2:p.Phe1502Leu
XM_005272018.3:c.3904T>C XP_005272075.1:p.Phe1302Leu
XM_011543488.1:c.4372T>C XP_011541790.1:p.Phe1458Leu
XM_011543489.1:c.4360T>C XP_011541791.1:p.Phe1454Leu
XM_005272018.4:c.3904T>C XP_005272075.1:p.Phe1302Leu
XM_011543488.2:c.4372T>C XP_011541790.1:p.Phe1458Leu
XM_011543489.2:c.4360T>C XP_011541791.1:p.Phe1454Leu
XM_017009584.1:c.3757T>C XP_016865073.1:p.Phe1253Leu
XM_024446115.1:c.4030T>C XP_024301883.1:p.Phe1344Leu
NM_016604.4:c.4504T>C MANE Select NP_057688.3:p.Phe1502Leu