Canonical Allele Identifier: CA507308309

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223720A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732819A>G , CM000681.2:g.35732819A>G	GRCh38
NC_000019.9:g.36223720A>G , CM000681.1:g.36223720A>G	GRCh37
NC_000019.8:g.40915560A>G	NCBI36
NG_052906.1:g.19801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.576A>G
ENST00000673918.2:c.6204A>G	ENSP00000501283.1:p.Val2068=
ENST00000674114.2:c.3811A>G	ENSP00000501039.2:n.3811A>G
ENST00000684977.1:c.1488A>G	ENSP00000509384.1:p.Val496=
ENST00000689544.1:n.1423A>G
ENST00000691421.1:c.1491A>G	ENSP00000508674.1:p.Val497=
ENST00000691855.1:c.5812A>G
ENST00000692961.1:c.6270A>G	ENSP00000509289.1:p.Val2090=
ENST00000693677.1:c.704+490A>G	ENSP00000509779.1:n.704+490A>G
ENST00000420124.4:c.6270A>G MANE Select	ENSP00000398837.2:p.Val2090=
ENST00000673918.1:c.6204A>G	ENSP00000501283.1:p.Val2068=
ENST00000674114.1:c.3592A>G
ENST00000420124.2:c.6270A>G	ENSP00000398837.1:p.Val2090=
NM_014727.2:c.6270A>G	NP_055542.1:p.Val2090=
XM_011527561.1:c.6204A>G	XP_011525863.1:p.Val2068=
XM_011527562.1:c.6270A>G	XP_011525864.1:p.Val2090=
XM_011527563.1:c.5994A>G	XP_011525865.1:p.Val1998=
XM_011527561.2:c.5706A>G	XP_011525863.2:p.Val1902=
XM_011527562.2:c.6270A>G	XP_011525864.1:p.Val2090=
XM_017027544.1:c.6270A>G	XP_016883033.1:p.Val2090=
XM_017027545.1:c.5706A>G	XP_016883034.1:p.Val1902=
XM_017027546.1:c.3234A>G	XP_016883035.1:p.Val1078=
NM_014727.3:c.6270A>G MANE Select	NP_055542.1:p.Val2090=