Canonical Allele Identifier: CA3650391

Gene: KDM1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18161328C>T , CM000668.2:g.18161328C>T	GRCh38
NC_000006.11:g.18161559C>T , CM000668.1:g.18161559C>T	GRCh37
NC_000006.10:g.18269538C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449850.2:c.89C>T	ENSP00000405669.2:p.Ala30Val
ENST00000650836.2:c.89C>T MANE Select	ENSP00000499208.1:p.Ala30Val
ENST00000297792.9:c.89C>T	ENSP00000297792.5:p.Ala30Val
ENST00000546309.6:c.-19+5915C>T	ENSP00000442670.1:n.-19+5915C>T
NM_153042.3:c.89C>T	NP_694587.3:p.Ala30Val
XM_005248925.1:c.89C>T	XP_005248982.1:p.Ala30Val
XM_005248926.1:c.89C>T	XP_005248983.1:p.Ala30Val
XM_005248927.1:c.89C>T	XP_005248984.1:p.Ala30Val
XM_005248928.1:c.89C>T	XP_005248985.1:p.Ala30Val
XM_005248929.2:c.89C>T	XP_005248986.1:p.Ala30Val
XM_011514385.1:c.89C>T	XP_011512687.1:p.Ala30Val
XM_011514386.1:c.89C>T	XP_011512688.1:p.Ala30Val
NM_001364614.1:c.89C>T	NP_001351543.1:p.Ala30Val
XM_005248925.2:c.89C>T	XP_005248982.1:p.Ala30Val
XM_005248926.2:c.89C>T	XP_005248983.1:p.Ala30Val
XM_005248928.2:c.89C>T	XP_005248985.1:p.Ala30Val
XM_011514385.2:c.89C>T	XP_011512687.1:p.Ala30Val
XM_011514386.2:c.89C>T	XP_011512688.1:p.Ala30Val
XM_017010440.2:c.89C>T	XP_016865929.1:p.Ala30Val
XM_017010441.2:c.89C>T	XP_016865930.1:p.Ala30Val
XM_017010442.2:c.89C>T	XP_016865931.1:p.Ala30Val
XM_017010443.2:c.89C>T	XP_016865932.1:p.Ala30Val
XM_017010445.2:c.89C>T	XP_016865934.1:p.Ala30Val
XM_017010446.1:c.89C>T	XP_016865935.1:p.Ala30Val
NM_001364614.2:c.89C>T MANE Select	NP_001351543.1:p.Ala30Val
NM_153042.4:c.89C>T	NP_694587.3:p.Ala30Val