Canonical Allele Identifier: CA405428285

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223851A>C (hg19) ; chr19:g.35732950A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732950A>C , CM000681.2:g.35732950A>C	GRCh38
NC_000019.9:g.36223851A>C , CM000681.1:g.36223851A>C	GRCh37
NC_000019.8:g.40915691A>C	NCBI36
NG_052906.1:g.19932A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.707A>C
ENST00000673918.2:c.6335A>C	ENSP00000501283.1:p.Glu2112Ala
ENST00000674114.2:c.3942A>C	ENSP00000501039.2:n.3942A>C
ENST00000684977.1:c.1619A>C	ENSP00000509384.1:p.Glu540Ala
ENST00000689544.1:n.1554A>C
ENST00000691421.1:c.1622A>C	ENSP00000508674.1:p.Glu541Ala
ENST00000691855.1:c.5943A>C
ENST00000692961.1:c.6401A>C	ENSP00000509289.1:p.Glu2134Ala
ENST00000693677.1:c.704+621A>C	ENSP00000509779.1:n.704+621A>C
ENST00000420124.4:c.6401A>C MANE Select	ENSP00000398837.2:p.Glu2134Ala
ENST00000673918.1:c.6335A>C	ENSP00000501283.1:p.Glu2112Ala
ENST00000674114.1:c.3723A>C
ENST00000420124.2:c.6401A>C	ENSP00000398837.1:p.Glu2134Ala
NM_014727.2:c.6401A>C	NP_055542.1:p.Glu2134Ala
XM_011527561.1:c.6335A>C	XP_011525863.1:p.Glu2112Ala
XM_011527562.1:c.6401A>C	XP_011525864.1:p.Glu2134Ala
XM_011527563.1:c.6125A>C	XP_011525865.1:p.Glu2042Ala
XM_011527561.2:c.5837A>C	XP_011525863.2:p.Glu1946Ala
XM_011527562.2:c.6401A>C	XP_011525864.1:p.Glu2134Ala
XM_017027544.1:c.6401A>C	XP_016883033.1:p.Glu2134Ala
XM_017027545.1:c.5837A>C	XP_016883034.1:p.Glu1946Ala
XM_017027546.1:c.3365A>C	XP_016883035.1:p.Glu1122Ala
NM_014727.3:c.6401A>C MANE Select	NP_055542.1:p.Glu2134Ala