Canonical Allele Identifier: CA405428105

Gene: KMT2B

Linked Data

• dbSNP Id: rs1449834886
• gnomAD v2: 19-36223824-G-A
• MyVariant Identifiers: chr19:g.36223824G>A (hg19) ; chr19:g.35732923G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732923G>A , CM000681.2:g.35732923G>A	GRCh38
NC_000019.9:g.36223824G>A , CM000681.1:g.36223824G>A	GRCh37
NC_000019.8:g.40915664G>A	NCBI36
NG_052906.1:g.19905G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.680G>A
ENST00000673918.2:c.6308G>A	ENSP00000501283.1:p.Gly2103Glu
ENST00000674114.2:c.3915G>A	ENSP00000501039.2:n.3915G>A
ENST00000684977.1:c.1592G>A	ENSP00000509384.1:p.Gly531Glu
ENST00000689544.1:n.1527G>A
ENST00000691421.1:c.1595G>A	ENSP00000508674.1:p.Gly532Glu
ENST00000691855.1:c.5916G>A
ENST00000692961.1:c.6374G>A	ENSP00000509289.1:p.Gly2125Glu
ENST00000693677.1:c.704+594G>A	ENSP00000509779.1:n.704+594G>A
ENST00000420124.4:c.6374G>A MANE Select	ENSP00000398837.2:p.Gly2125Glu
ENST00000673918.1:c.6308G>A	ENSP00000501283.1:p.Gly2103Glu
ENST00000674114.1:c.3696G>A
ENST00000420124.2:c.6374G>A	ENSP00000398837.1:p.Gly2125Glu
NM_014727.2:c.6374G>A	NP_055542.1:p.Gly2125Glu
XM_011527561.1:c.6308G>A	XP_011525863.1:p.Gly2103Glu
XM_011527562.1:c.6374G>A	XP_011525864.1:p.Gly2125Glu
XM_011527563.1:c.6098G>A	XP_011525865.1:p.Gly2033Glu
XM_011527561.2:c.5810G>A	XP_011525863.2:p.Gly1937Glu
XM_011527562.2:c.6374G>A	XP_011525864.1:p.Gly2125Glu
XM_017027544.1:c.6374G>A	XP_016883033.1:p.Gly2125Glu
XM_017027545.1:c.5810G>A	XP_016883034.1:p.Gly1937Glu
XM_017027546.1:c.3338G>A	XP_016883035.1:p.Gly1113Glu
NM_014727.3:c.6374G>A MANE Select	NP_055542.1:p.Gly2125Glu