Canonical Allele Identifier: CA507308205

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223462G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732561G>A , CM000681.2:g.35732561G>A	GRCh38
NC_000019.9:g.36223462G>A , CM000681.1:g.36223462G>A	GRCh37
NC_000019.8:g.40915302G>A	NCBI36
NG_052906.1:g.19543G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.318G>A
ENST00000673918.2:c.5946G>A	ENSP00000501283.1:p.Gln1982=
ENST00000674114.2:c.3553G>A	ENSP00000501039.2:n.3553G>A
ENST00000684977.1:c.1230G>A	ENSP00000509384.1:p.Gln410=
ENST00000689544.1:n.1165G>A
ENST00000691421.1:c.1233G>A	ENSP00000508674.1:p.Gln411=
ENST00000691855.1:c.5554G>A
ENST00000692961.1:c.6012G>A	ENSP00000509289.1:p.Gln2004=
ENST00000693677.1:c.704+232G>A	ENSP00000509779.1:n.704+232G>A
ENST00000420124.4:c.6012G>A MANE Select	ENSP00000398837.2:p.Gln2004=
ENST00000673918.1:c.5946G>A	ENSP00000501283.1:p.Gln1982=
ENST00000674114.1:c.3334G>A
ENST00000420124.2:c.6012G>A	ENSP00000398837.1:p.Gln2004=
NM_014727.2:c.6012G>A	NP_055542.1:p.Gln2004=
XM_011527561.1:c.5946G>A	XP_011525863.1:p.Gln1982=
XM_011527562.1:c.6012G>A	XP_011525864.1:p.Gln2004=
XM_011527563.1:c.5736G>A	XP_011525865.1:p.Gln1912=
XM_011527561.2:c.5448G>A	XP_011525863.2:p.Gln1816=
XM_011527562.2:c.6012G>A	XP_011525864.1:p.Gln2004=
XM_017027544.1:c.6012G>A	XP_016883033.1:p.Gln2004=
XM_017027545.1:c.5448G>A	XP_016883034.1:p.Gln1816=
XM_017027546.1:c.2976G>A	XP_016883035.1:p.Gln992=
NM_014727.3:c.6012G>A MANE Select	NP_055542.1:p.Gln2004=