Canonical Allele Identifier: CA507308088

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223396G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732495G>A , CM000681.2:g.35732495G>A	GRCh38
NC_000019.9:g.36223396G>A , CM000681.1:g.36223396G>A	GRCh37
NC_000019.8:g.40915236G>A	NCBI36
NG_052906.1:g.19477G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.252G>A
ENST00000673918.2:c.5880G>A	ENSP00000501283.1:p.Val1960=
ENST00000674114.2:c.3487G>A	ENSP00000501039.2:n.3487G>A
ENST00000684977.1:c.1164G>A	ENSP00000509384.1:p.Val388=
ENST00000689544.1:n.1099G>A
ENST00000691421.1:c.1167G>A	ENSP00000508674.1:p.Val389=
ENST00000691855.1:c.5488G>A
ENST00000692961.1:c.5946G>A	ENSP00000509289.1:p.Val1982=
ENST00000693677.1:c.704+166G>A	ENSP00000509779.1:n.704+166G>A
ENST00000420124.4:c.5946G>A MANE Select	ENSP00000398837.2:p.Val1982=
ENST00000673918.1:c.5880G>A	ENSP00000501283.1:p.Val1960=
ENST00000674114.1:c.3268G>A
ENST00000420124.2:c.5946G>A	ENSP00000398837.1:p.Val1982=
NM_014727.2:c.5946G>A	NP_055542.1:p.Val1982=
XM_011527561.1:c.5880G>A	XP_011525863.1:p.Val1960=
XM_011527562.1:c.5946G>A	XP_011525864.1:p.Val1982=
XM_011527563.1:c.5670G>A	XP_011525865.1:p.Val1890=
XM_011527561.2:c.5382G>A	XP_011525863.2:p.Val1794=
XM_011527562.2:c.5946G>A	XP_011525864.1:p.Val1982=
XM_017027544.1:c.5946G>A	XP_016883033.1:p.Val1982=
XM_017027545.1:c.5382G>A	XP_016883034.1:p.Val1794=
XM_017027546.1:c.2910G>A	XP_016883035.1:p.Val970=
NM_014727.3:c.5946G>A MANE Select	NP_055542.1:p.Val1982=