Canonical Allele Identifier: CA405419374

Gene: KMT2B

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730341G>A , CM000681.2:g.35730341G>A	GRCh38
NC_000019.9:g.36221242G>A , CM000681.1:g.36221242G>A	GRCh37
NC_000019.8:g.40913082G>A	NCBI36
NG_052906.1:g.17323G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.5011-1G>A	ENSP00000501283.1:n.5011-1G>A
ENST00000674114.2:c.2618-1G>A	ENSP00000501039.2:n.2618-1G>A
ENST00000684977.1:c.295-1G>A	ENSP00000509384.1:n.295-1G>A
ENST00000685168.1:c.503-1G>A
ENST00000689544.1:n.230-1G>A
ENST00000691421.1:c.298-1G>A	ENSP00000508674.1:n.298-1G>A
ENST00000691855.1:c.4619-1G>A
ENST00000692961.1:c.5077-1G>A	ENSP00000509289.1:n.5077-1G>A
ENST00000420124.4:c.5077-1G>A MANE Select	ENSP00000398837.2:n.5077-1G>A
ENST00000673918.1:c.5011-1G>A	ENSP00000501283.1:n.5011-1G>A
ENST00000674114.1:c.2399-1G>A
ENST00000420124.2:c.5077-1G>A	ENSP00000398837.1:n.5077-1G>A
NM_014727.2:c.5077-1G>A	NP_055542.1:n.5077-1G>A
XM_011527561.1:c.5011-1G>A	XP_011525863.1:n.5011-1G>A
XM_011527562.1:c.5077-1G>A	XP_011525864.1:n.5077-1G>A
XM_011527563.1:c.4801-1G>A	XP_011525865.1:n.4801-1G>A
XM_011527561.2:c.4513-1G>A	XP_011525863.2:n.4513-1G>A
XM_011527562.2:c.5077-1G>A	XP_011525864.1:n.5077-1G>A
XM_017027544.1:c.5077-1G>A	XP_016883033.1:n.5077-1G>A
XM_017027545.1:c.4513-1G>A	XP_016883034.1:n.4513-1G>A
XM_017027546.1:c.2041-1G>A	XP_016883035.1:n.2041-1G>A
NM_014727.3:c.5077-1G>A MANE Select	NP_055542.1:n.5077-1G>A