Canonical Allele Identifier: CA405427462

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732823-C-G
• MyVariant Identifiers: chr19:g.36223724C>G (hg19) ; chr19:g.35732823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732823C>G , CM000681.2:g.35732823C>G	GRCh38
NC_000019.9:g.36223724C>G , CM000681.1:g.36223724C>G	GRCh37
NC_000019.8:g.40915564C>G	NCBI36
NG_052906.1:g.19805C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.580C>G
ENST00000673918.2:c.6208C>G	ENSP00000501283.1:p.Arg2070Gly
ENST00000674114.2:c.3815C>G	ENSP00000501039.2:n.3815C>G
ENST00000684977.1:c.1492C>G	ENSP00000509384.1:p.Arg498Gly
ENST00000689544.1:n.1427C>G
ENST00000691421.1:c.1495C>G	ENSP00000508674.1:p.Arg499Gly
ENST00000691855.1:c.5816C>G
ENST00000692961.1:c.6274C>G	ENSP00000509289.1:p.Arg2092Gly
ENST00000693677.1:c.704+494C>G	ENSP00000509779.1:n.704+494C>G
ENST00000420124.4:c.6274C>G MANE Select	ENSP00000398837.2:p.Arg2092Gly
ENST00000673918.1:c.6208C>G	ENSP00000501283.1:p.Arg2070Gly
ENST00000674114.1:c.3596C>G
ENST00000420124.2:c.6274C>G	ENSP00000398837.1:p.Arg2092Gly
NM_014727.2:c.6274C>G	NP_055542.1:p.Arg2092Gly
XM_011527561.1:c.6208C>G	XP_011525863.1:p.Arg2070Gly
XM_011527562.1:c.6274C>G	XP_011525864.1:p.Arg2092Gly
XM_011527563.1:c.5998C>G	XP_011525865.1:p.Arg2000Gly
XM_011527561.2:c.5710C>G	XP_011525863.2:p.Arg1904Gly
XM_011527562.2:c.6274C>G	XP_011525864.1:p.Arg2092Gly
XM_017027544.1:c.6274C>G	XP_016883033.1:p.Arg2092Gly
XM_017027545.1:c.5710C>G	XP_016883034.1:p.Arg1904Gly
XM_017027546.1:c.3238C>G	XP_016883035.1:p.Arg1080Gly
NM_014727.3:c.6274C>G MANE Select	NP_055542.1:p.Arg2092Gly