Canonical Allele Identifier: CA405427926

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223795T>A (hg19) ; chr19:g.35732894T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732894T>A , CM000681.2:g.35732894T>A	GRCh38
NC_000019.9:g.36223795T>A , CM000681.1:g.36223795T>A	GRCh37
NC_000019.8:g.40915635T>A	NCBI36
NG_052906.1:g.19876T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.651T>A
ENST00000673918.2:c.6279T>A	ENSP00000501283.1:p.Asp2093Glu
ENST00000674114.2:c.3886T>A	ENSP00000501039.2:n.3886T>A
ENST00000684977.1:c.1563T>A	ENSP00000509384.1:p.Asp521Glu
ENST00000689544.1:n.1498T>A
ENST00000691421.1:c.1566T>A	ENSP00000508674.1:p.Asp522Glu
ENST00000691855.1:c.5887T>A
ENST00000692961.1:c.6345T>A	ENSP00000509289.1:p.Asp2115Glu
ENST00000693677.1:c.704+565T>A	ENSP00000509779.1:n.704+565T>A
ENST00000420124.4:c.6345T>A MANE Select	ENSP00000398837.2:p.Asp2115Glu
ENST00000673918.1:c.6279T>A	ENSP00000501283.1:p.Asp2093Glu
ENST00000674114.1:c.3667T>A
ENST00000420124.2:c.6345T>A	ENSP00000398837.1:p.Asp2115Glu
NM_014727.2:c.6345T>A	NP_055542.1:p.Asp2115Glu
XM_011527561.1:c.6279T>A	XP_011525863.1:p.Asp2093Glu
XM_011527562.1:c.6345T>A	XP_011525864.1:p.Asp2115Glu
XM_011527563.1:c.6069T>A	XP_011525865.1:p.Asp2023Glu
XM_011527561.2:c.5781T>A	XP_011525863.2:p.Asp1927Glu
XM_011527562.2:c.6345T>A	XP_011525864.1:p.Asp2115Glu
XM_017027544.1:c.6345T>A	XP_016883033.1:p.Asp2115Glu
XM_017027545.1:c.5781T>A	XP_016883034.1:p.Asp1927Glu
XM_017027546.1:c.3309T>A	XP_016883035.1:p.Asp1103Glu
NM_014727.3:c.6345T>A MANE Select	NP_055542.1:p.Asp2115Glu