Canonical Allele Identifier: CA507308084

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732477-C-T
• MyVariant Identifiers: chr19:g.36223378C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732477C>T , CM000681.2:g.35732477C>T	GRCh38
NC_000019.9:g.36223378C>T , CM000681.1:g.36223378C>T	GRCh37
NC_000019.8:g.40915218C>T	NCBI36
NG_052906.1:g.19459C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.234C>T
ENST00000673918.2:c.5862C>T	ENSP00000501283.1:p.Asp1954=
ENST00000674114.2:c.3469C>T	ENSP00000501039.2:n.3469C>T
ENST00000684977.1:c.1146C>T	ENSP00000509384.1:p.Asp382=
ENST00000689544.1:n.1081C>T
ENST00000691421.1:c.1149C>T	ENSP00000508674.1:p.Asp383=
ENST00000691855.1:c.5470C>T
ENST00000692961.1:c.5928C>T	ENSP00000509289.1:p.Asp1976=
ENST00000693677.1:c.704+148C>T	ENSP00000509779.1:n.704+148C>T
ENST00000420124.4:c.5928C>T MANE Select	ENSP00000398837.2:p.Asp1976=
ENST00000673918.1:c.5862C>T	ENSP00000501283.1:p.Asp1954=
ENST00000674114.1:c.3250C>T
ENST00000420124.2:c.5928C>T	ENSP00000398837.1:p.Asp1976=
NM_014727.2:c.5928C>T	NP_055542.1:p.Asp1976=
XM_011527561.1:c.5862C>T	XP_011525863.1:p.Asp1954=
XM_011527562.1:c.5928C>T	XP_011525864.1:p.Asp1976=
XM_011527563.1:c.5652C>T	XP_011525865.1:p.Asp1884=
XM_011527561.2:c.5364C>T	XP_011525863.2:p.Asp1788=
XM_011527562.2:c.5928C>T	XP_011525864.1:p.Asp1976=
XM_017027544.1:c.5928C>T	XP_016883033.1:p.Asp1976=
XM_017027545.1:c.5364C>T	XP_016883034.1:p.Asp1788=
XM_017027546.1:c.2892C>T	XP_016883035.1:p.Asp964=
NM_014727.3:c.5928C>T MANE Select	NP_055542.1:p.Asp1976=