Canonical Allele Identifier: CA507308641

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223801G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732900G>A , CM000681.2:g.35732900G>A	GRCh38
NC_000019.9:g.36223801G>A , CM000681.1:g.36223801G>A	GRCh37
NC_000019.8:g.40915641G>A	NCBI36
NG_052906.1:g.19882G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.657G>A
ENST00000673918.2:c.6285G>A	ENSP00000501283.1:p.Val2095=
ENST00000674114.2:c.3892G>A	ENSP00000501039.2:n.3892G>A
ENST00000684977.1:c.1569G>A	ENSP00000509384.1:p.Val523=
ENST00000689544.1:n.1504G>A
ENST00000691421.1:c.1572G>A	ENSP00000508674.1:p.Val524=
ENST00000691855.1:c.5893G>A
ENST00000692961.1:c.6351G>A	ENSP00000509289.1:p.Val2117=
ENST00000693677.1:c.704+571G>A	ENSP00000509779.1:n.704+571G>A
ENST00000420124.4:c.6351G>A MANE Select	ENSP00000398837.2:p.Val2117=
ENST00000673918.1:c.6285G>A	ENSP00000501283.1:p.Val2095=
ENST00000674114.1:c.3673G>A
ENST00000420124.2:c.6351G>A	ENSP00000398837.1:p.Val2117=
NM_014727.2:c.6351G>A	NP_055542.1:p.Val2117=
XM_011527561.1:c.6285G>A	XP_011525863.1:p.Val2095=
XM_011527562.1:c.6351G>A	XP_011525864.1:p.Val2117=
XM_011527563.1:c.6075G>A	XP_011525865.1:p.Val2025=
XM_011527561.2:c.5787G>A	XP_011525863.2:p.Val1929=
XM_011527562.2:c.6351G>A	XP_011525864.1:p.Val2117=
XM_017027544.1:c.6351G>A	XP_016883033.1:p.Val2117=
XM_017027545.1:c.5787G>A	XP_016883034.1:p.Val1929=
XM_017027546.1:c.3315G>A	XP_016883035.1:p.Val1105=
NM_014727.3:c.6351G>A MANE Select	NP_055542.1:p.Val2117=