Canonical Allele Identifier: CA405427551

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223739G>A (hg19) ; chr19:g.35732838G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732838G>A , CM000681.2:g.35732838G>A	GRCh38
NC_000019.9:g.36223739G>A , CM000681.1:g.36223739G>A	GRCh37
NC_000019.8:g.40915579G>A	NCBI36
NG_052906.1:g.19820G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.595G>A
ENST00000673918.2:c.6223G>A	ENSP00000501283.1:p.Gly2075Arg
ENST00000674114.2:c.3830G>A	ENSP00000501039.2:n.3830G>A
ENST00000684977.1:c.1507G>A	ENSP00000509384.1:p.Gly503Arg
ENST00000689544.1:n.1442G>A
ENST00000691421.1:c.1510G>A	ENSP00000508674.1:p.Gly504Arg
ENST00000691855.1:c.5831G>A
ENST00000692961.1:c.6289G>A	ENSP00000509289.1:p.Gly2097Arg
ENST00000693677.1:c.704+509G>A	ENSP00000509779.1:n.704+509G>A
ENST00000420124.4:c.6289G>A MANE Select	ENSP00000398837.2:p.Gly2097Arg
ENST00000673918.1:c.6223G>A	ENSP00000501283.1:p.Gly2075Arg
ENST00000674114.1:c.3611G>A
ENST00000420124.2:c.6289G>A	ENSP00000398837.1:p.Gly2097Arg
NM_014727.2:c.6289G>A	NP_055542.1:p.Gly2097Arg
XM_011527561.1:c.6223G>A	XP_011525863.1:p.Gly2075Arg
XM_011527562.1:c.6289G>A	XP_011525864.1:p.Gly2097Arg
XM_011527563.1:c.6013G>A	XP_011525865.1:p.Gly2005Arg
XM_011527561.2:c.5725G>A	XP_011525863.2:p.Gly1909Arg
XM_011527562.2:c.6289G>A	XP_011525864.1:p.Gly2097Arg
XM_017027544.1:c.6289G>A	XP_016883033.1:p.Gly2097Arg
XM_017027545.1:c.5725G>A	XP_016883034.1:p.Gly1909Arg
XM_017027546.1:c.3253G>A	XP_016883035.1:p.Gly1085Arg
NM_014727.3:c.6289G>A MANE Select	NP_055542.1:p.Gly2097Arg