Canonical Allele Identifier: CA405427440

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223721G>A (hg19) ; chr19:g.35732820G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732820G>A , CM000681.2:g.35732820G>A	GRCh38
NC_000019.9:g.36223721G>A , CM000681.1:g.36223721G>A	GRCh37
NC_000019.8:g.40915561G>A	NCBI36
NG_052906.1:g.19802G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.577G>A
ENST00000673918.2:c.6205G>A	ENSP00000501283.1:p.Val2069Ile
ENST00000674114.2:c.3812G>A	ENSP00000501039.2:n.3812G>A
ENST00000684977.1:c.1489G>A	ENSP00000509384.1:p.Val497Ile
ENST00000689544.1:n.1424G>A
ENST00000691421.1:c.1492G>A	ENSP00000508674.1:p.Val498Ile
ENST00000691855.1:c.5813G>A
ENST00000692961.1:c.6271G>A	ENSP00000509289.1:p.Val2091Ile
ENST00000693677.1:c.704+491G>A	ENSP00000509779.1:n.704+491G>A
ENST00000420124.4:c.6271G>A MANE Select	ENSP00000398837.2:p.Val2091Ile
ENST00000673918.1:c.6205G>A	ENSP00000501283.1:p.Val2069Ile
ENST00000674114.1:c.3593G>A
ENST00000420124.2:c.6271G>A	ENSP00000398837.1:p.Val2091Ile
NM_014727.2:c.6271G>A	NP_055542.1:p.Val2091Ile
XM_011527561.1:c.6205G>A	XP_011525863.1:p.Val2069Ile
XM_011527562.1:c.6271G>A	XP_011525864.1:p.Val2091Ile
XM_011527563.1:c.5995G>A	XP_011525865.1:p.Val1999Ile
XM_011527561.2:c.5707G>A	XP_011525863.2:p.Val1903Ile
XM_011527562.2:c.6271G>A	XP_011525864.1:p.Val2091Ile
XM_017027544.1:c.6271G>A	XP_016883033.1:p.Val2091Ile
XM_017027545.1:c.5707G>A	XP_016883034.1:p.Val1903Ile
XM_017027546.1:c.3235G>A	XP_016883035.1:p.Val1079Ile
NM_014727.3:c.6271G>A MANE Select	NP_055542.1:p.Val2091Ile