Canonical Allele Identifier: CA405429426

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224042G>C (hg19) ; chr19:g.35733141G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733141G>C , CM000681.2:g.35733141G>C	GRCh38
NC_000019.9:g.36224042G>C , CM000681.1:g.36224042G>C	GRCh37
NC_000019.8:g.40915882G>C	NCBI36
NG_052906.1:g.20123G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.898G>C
ENST00000673918.2:c.6526G>C	ENSP00000501283.1:p.Gly2176Arg
ENST00000674114.2:c.4133G>C	ENSP00000501039.2:n.4133G>C
ENST00000684977.1:c.1810G>C	ENSP00000509384.1:p.Gly604Arg
ENST00000689544.1:n.1745G>C
ENST00000691421.1:c.1813G>C	ENSP00000508674.1:p.Gly605Arg
ENST00000691855.1:c.6134G>C
ENST00000692961.1:c.6592G>C	ENSP00000509289.1:p.Gly2198Arg
ENST00000693677.1:c.705-456G>C	ENSP00000509779.1:n.705-456G>C
ENST00000420124.4:c.6592G>C MANE Select	ENSP00000398837.2:p.Gly2198Arg
ENST00000673918.1:c.6526G>C	ENSP00000501283.1:p.Gly2176Arg
ENST00000674114.1:c.3914G>C
ENST00000420124.2:c.6592G>C	ENSP00000398837.1:p.Gly2198Arg
NM_014727.2:c.6592G>C	NP_055542.1:p.Gly2198Arg
XM_011527561.1:c.6526G>C	XP_011525863.1:p.Gly2176Arg
XM_011527562.1:c.6592G>C	XP_011525864.1:p.Gly2198Arg
XM_011527563.1:c.6316G>C	XP_011525865.1:p.Gly2106Arg
XM_011527561.2:c.6028G>C	XP_011525863.2:p.Gly2010Arg
XM_011527562.2:c.6592G>C	XP_011525864.1:p.Gly2198Arg
XM_017027544.1:c.6592G>C	XP_016883033.1:p.Gly2198Arg
XM_017027545.1:c.6028G>C	XP_016883034.1:p.Gly2010Arg
XM_017027546.1:c.3556G>C	XP_016883035.1:p.Gly1186Arg
NM_014727.3:c.6592G>C MANE Select	NP_055542.1:p.Gly2198Arg