Canonical Allele Identifier: CA405426052

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223659G>T (hg19) ; chr19:g.35732758G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732758G>T , CM000681.2:g.35732758G>T	GRCh38
NC_000019.9:g.36223659G>T , CM000681.1:g.36223659G>T	GRCh37
NC_000019.8:g.40915499G>T	NCBI36
NG_052906.1:g.19740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.515G>T
ENST00000673918.2:c.6143G>T	ENSP00000501283.1:p.Ser2048Ile
ENST00000674114.2:c.3750G>T	ENSP00000501039.2:n.3750G>T
ENST00000684977.1:c.1427G>T	ENSP00000509384.1:p.Ser476Ile
ENST00000689544.1:n.1362G>T
ENST00000691421.1:c.1430G>T	ENSP00000508674.1:p.Ser477Ile
ENST00000691855.1:c.5751G>T
ENST00000692961.1:c.6209G>T	ENSP00000509289.1:p.Ser2070Ile
ENST00000693677.1:c.704+429G>T	ENSP00000509779.1:n.704+429G>T
ENST00000420124.4:c.6209G>T MANE Select	ENSP00000398837.2:p.Ser2070Ile
ENST00000673918.1:c.6143G>T	ENSP00000501283.1:p.Ser2048Ile
ENST00000674114.1:c.3531G>T
ENST00000420124.2:c.6209G>T	ENSP00000398837.1:p.Ser2070Ile
NM_014727.2:c.6209G>T	NP_055542.1:p.Ser2070Ile
XM_011527561.1:c.6143G>T	XP_011525863.1:p.Ser2048Ile
XM_011527562.1:c.6209G>T	XP_011525864.1:p.Ser2070Ile
XM_011527563.1:c.5933G>T	XP_011525865.1:p.Ser1978Ile
XM_011527561.2:c.5645G>T	XP_011525863.2:p.Ser1882Ile
XM_011527562.2:c.6209G>T	XP_011525864.1:p.Ser2070Ile
XM_017027544.1:c.6209G>T	XP_016883033.1:p.Ser2070Ile
XM_017027545.1:c.5645G>T	XP_016883034.1:p.Ser1882Ile
XM_017027546.1:c.3173G>T	XP_016883035.1:p.Ser1058Ile
NM_014727.3:c.6209G>T MANE Select	NP_055542.1:p.Ser2070Ile