Canonical Allele Identifier: CA507308972

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223891G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732990G>A , CM000681.2:g.35732990G>A	GRCh38
NC_000019.9:g.36223891G>A , CM000681.1:g.36223891G>A	GRCh37
NC_000019.8:g.40915731G>A	NCBI36
NG_052906.1:g.19972G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.747G>A
ENST00000673918.2:c.6375G>A	ENSP00000501283.1:p.Gln2125=
ENST00000674114.2:c.3982G>A	ENSP00000501039.2:n.3982G>A
ENST00000684977.1:c.1659G>A	ENSP00000509384.1:p.Gln553=
ENST00000689544.1:n.1594G>A
ENST00000691421.1:c.1662G>A	ENSP00000508674.1:p.Gln554=
ENST00000691855.1:c.5983G>A
ENST00000692961.1:c.6441G>A	ENSP00000509289.1:p.Gln2147=
ENST00000693677.1:c.705-607G>A	ENSP00000509779.1:n.705-607G>A
ENST00000420124.4:c.6441G>A MANE Select	ENSP00000398837.2:p.Gln2147=
ENST00000673918.1:c.6375G>A	ENSP00000501283.1:p.Gln2125=
ENST00000674114.1:c.3763G>A
ENST00000420124.2:c.6441G>A	ENSP00000398837.1:p.Gln2147=
NM_014727.2:c.6441G>A	NP_055542.1:p.Gln2147=
XM_011527561.1:c.6375G>A	XP_011525863.1:p.Gln2125=
XM_011527562.1:c.6441G>A	XP_011525864.1:p.Gln2147=
XM_011527563.1:c.6165G>A	XP_011525865.1:p.Gln2055=
XM_011527561.2:c.5877G>A	XP_011525863.2:p.Gln1959=
XM_011527562.2:c.6441G>A	XP_011525864.1:p.Gln2147=
XM_017027544.1:c.6441G>A	XP_016883033.1:p.Gln2147=
XM_017027545.1:c.5877G>A	XP_016883034.1:p.Gln1959=
XM_017027546.1:c.3405G>A	XP_016883035.1:p.Gln1135=
NM_014727.3:c.6441G>A MANE Select	NP_055542.1:p.Gln2147=