Canonical Allele Identifier: CA507073952

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224763C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733862C>T , CM000681.2:g.35733862C>T	GRCh38
NC_000019.9:g.36224763C>T , CM000681.1:g.36224763C>T	GRCh37
NC_000019.8:g.40916603C>T	NCBI36
NG_052906.1:g.20844C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.1619C>T
ENST00000673918.2:c.7083C>T	ENSP00000501283.1:p.His2361=
ENST00000674114.2:c.4690C>T	ENSP00000501039.2:n.4690C>T
ENST00000684977.1:c.2344C>T	ENSP00000509384.1:n.2344C>T
ENST00000689544.1:n.2390C>T
ENST00000689929.1:c.100C>T
ENST00000691421.1:c.2280C>T	ENSP00000508674.1:p.His760=
ENST00000691855.1:c.6691C>T
ENST00000692961.1:c.7073C>T	ENSP00000509289.1:p.Thr2358Ile
ENST00000693175.1:c.100C>T
ENST00000693677.1:c.894C>T	ENSP00000509779.1:p.His298=
ENST00000420124.4:c.7149C>T MANE Select	ENSP00000398837.2:p.His2383=
ENST00000673918.1:c.7083C>T	ENSP00000501283.1:p.His2361=
ENST00000674114.1:c.4471C>T
ENST00000420124.2:c.7149C>T	ENSP00000398837.1:p.His2383=
ENST00000592092.1:n.529C>T
NM_014727.2:c.7149C>T	NP_055542.1:p.His2383=
XM_011527561.1:c.7083C>T	XP_011525863.1:p.His2361=
XM_011527562.1:c.7149C>T	XP_011525864.1:p.His2383=
XM_011527563.1:c.6873C>T	XP_011525865.1:p.His2291=
XM_011527561.2:c.6585C>T	XP_011525863.2:p.His2195=
XM_011527562.2:c.7149C>T	XP_011525864.1:p.His2383=
XM_017027544.1:c.7059C>T	XP_016883033.1:p.His2353=
XM_017027545.1:c.6585C>T	XP_016883034.1:p.His2195=
XM_017027546.1:c.4113C>T	XP_016883035.1:p.His1371=
NM_014727.3:c.7149C>T MANE Select	NP_055542.1:p.His2383=