Canonical Allele Identifier: CA507308849

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223678G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732777G>A , CM000681.2:g.35732777G>A	GRCh38
NC_000019.9:g.36223678G>A , CM000681.1:g.36223678G>A	GRCh37
NC_000019.8:g.40915518G>A	NCBI36
NG_052906.1:g.19759G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.534G>A
ENST00000673918.2:c.6162G>A	ENSP00000501283.1:p.Gln2054=
ENST00000674114.2:c.3769G>A	ENSP00000501039.2:n.3769G>A
ENST00000684977.1:c.1446G>A	ENSP00000509384.1:p.Gln482=
ENST00000689544.1:n.1381G>A
ENST00000691421.1:c.1449G>A	ENSP00000508674.1:p.Gln483=
ENST00000691855.1:c.5770G>A
ENST00000692961.1:c.6228G>A	ENSP00000509289.1:p.Gln2076=
ENST00000693677.1:c.704+448G>A	ENSP00000509779.1:n.704+448G>A
ENST00000420124.4:c.6228G>A MANE Select	ENSP00000398837.2:p.Gln2076=
ENST00000673918.1:c.6162G>A	ENSP00000501283.1:p.Gln2054=
ENST00000674114.1:c.3550G>A
ENST00000420124.2:c.6228G>A	ENSP00000398837.1:p.Gln2076=
NM_014727.2:c.6228G>A	NP_055542.1:p.Gln2076=
XM_011527561.1:c.6162G>A	XP_011525863.1:p.Gln2054=
XM_011527562.1:c.6228G>A	XP_011525864.1:p.Gln2076=
XM_011527563.1:c.5952G>A	XP_011525865.1:p.Gln1984=
XM_011527561.2:c.5664G>A	XP_011525863.2:p.Gln1888=
XM_011527562.2:c.6228G>A	XP_011525864.1:p.Gln2076=
XM_017027544.1:c.6228G>A	XP_016883033.1:p.Gln2076=
XM_017027545.1:c.5664G>A	XP_016883034.1:p.Gln1888=
XM_017027546.1:c.3192G>A	XP_016883035.1:p.Gln1064=
NM_014727.3:c.6228G>A MANE Select	NP_055542.1:p.Gln2076=