Canonical Allele Identifier: CA405424877

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223419A>T (hg19) ; chr19:g.35732518A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732518A>T , CM000681.2:g.35732518A>T	GRCh38
NC_000019.9:g.36223419A>T , CM000681.1:g.36223419A>T	GRCh37
NC_000019.8:g.40915259A>T	NCBI36
NG_052906.1:g.19500A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.275A>T
ENST00000673918.2:c.5903A>T	ENSP00000501283.1:p.Asp1968Val
ENST00000674114.2:c.3510A>T	ENSP00000501039.2:n.3510A>T
ENST00000684977.1:c.1187A>T	ENSP00000509384.1:p.Asp396Val
ENST00000689544.1:n.1122A>T
ENST00000691421.1:c.1190A>T	ENSP00000508674.1:p.Asp397Val
ENST00000691855.1:c.5511A>T
ENST00000692961.1:c.5969A>T	ENSP00000509289.1:p.Asp1990Val
ENST00000693677.1:c.704+189A>T	ENSP00000509779.1:n.704+189A>T
ENST00000420124.4:c.5969A>T MANE Select	ENSP00000398837.2:p.Asp1990Val
ENST00000673918.1:c.5903A>T	ENSP00000501283.1:p.Asp1968Val
ENST00000674114.1:c.3291A>T
ENST00000420124.2:c.5969A>T	ENSP00000398837.1:p.Asp1990Val
NM_014727.2:c.5969A>T	NP_055542.1:p.Asp1990Val
XM_011527561.1:c.5903A>T	XP_011525863.1:p.Asp1968Val
XM_011527562.1:c.5969A>T	XP_011525864.1:p.Asp1990Val
XM_011527563.1:c.5693A>T	XP_011525865.1:p.Asp1898Val
XM_011527561.2:c.5405A>T	XP_011525863.2:p.Asp1802Val
XM_011527562.2:c.5969A>T	XP_011525864.1:p.Asp1990Val
XM_017027544.1:c.5969A>T	XP_016883033.1:p.Asp1990Val
XM_017027545.1:c.5405A>T	XP_016883034.1:p.Asp1802Val
XM_017027546.1:c.2933A>T	XP_016883035.1:p.Asp978Val
NM_014727.3:c.5969A>T MANE Select	NP_055542.1:p.Asp1990Val