Canonical Allele Identifier: CA405427633

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732850-G-T
• MyVariant Identifiers: chr19:g.36223751G>T (hg19) ; chr19:g.35732850G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732850G>T , CM000681.2:g.35732850G>T	GRCh38
NC_000019.9:g.36223751G>T , CM000681.1:g.36223751G>T	GRCh37
NC_000019.8:g.40915591G>T	NCBI36
NG_052906.1:g.19832G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.607G>T
ENST00000673918.2:c.6235G>T	ENSP00000501283.1:p.Asp2079Tyr
ENST00000674114.2:c.3842G>T	ENSP00000501039.2:n.3842G>T
ENST00000684977.1:c.1519G>T	ENSP00000509384.1:p.Asp507Tyr
ENST00000689544.1:n.1454G>T
ENST00000691421.1:c.1522G>T	ENSP00000508674.1:p.Asp508Tyr
ENST00000691855.1:c.5843G>T
ENST00000692961.1:c.6301G>T	ENSP00000509289.1:p.Asp2101Tyr
ENST00000693677.1:c.704+521G>T	ENSP00000509779.1:n.704+521G>T
ENST00000420124.4:c.6301G>T MANE Select	ENSP00000398837.2:p.Asp2101Tyr
ENST00000673918.1:c.6235G>T	ENSP00000501283.1:p.Asp2079Tyr
ENST00000674114.1:c.3623G>T
ENST00000420124.2:c.6301G>T	ENSP00000398837.1:p.Asp2101Tyr
NM_014727.2:c.6301G>T	NP_055542.1:p.Asp2101Tyr
XM_011527561.1:c.6235G>T	XP_011525863.1:p.Asp2079Tyr
XM_011527562.1:c.6301G>T	XP_011525864.1:p.Asp2101Tyr
XM_011527563.1:c.6025G>T	XP_011525865.1:p.Asp2009Tyr
XM_011527561.2:c.5737G>T	XP_011525863.2:p.Asp1913Tyr
XM_011527562.2:c.6301G>T	XP_011525864.1:p.Asp2101Tyr
XM_017027544.1:c.6301G>T	XP_016883033.1:p.Asp2101Tyr
XM_017027545.1:c.5737G>T	XP_016883034.1:p.Asp1913Tyr
XM_017027546.1:c.3265G>T	XP_016883035.1:p.Asp1089Tyr
NM_014727.3:c.6301G>T MANE Select	NP_055542.1:p.Asp2101Tyr