Canonical Allele Identifier: CA405431452

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224663G>A (hg19) ; chr19:g.35733762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733762G>A , CM000681.2:g.35733762G>A	GRCh38
NC_000019.9:g.36224663G>A , CM000681.1:g.36224663G>A	GRCh37
NC_000019.8:g.40916503G>A	NCBI36
NG_052906.1:g.20744G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.1519G>A
ENST00000673918.2:c.6984-1G>A	ENSP00000501283.1:n.6984-1G>A
ENST00000674114.2:c.4591-1G>A	ENSP00000501039.2:n.4591-1G>A
ENST00000684977.1:c.2245-1G>A	ENSP00000509384.1:n.2245-1G>A
ENST00000689544.1:n.2291-1G>A
ENST00000691421.1:c.2181-1G>A	ENSP00000508674.1:n.2181-1G>A
ENST00000691855.1:c.6592-1G>A
ENST00000692961.1:c.6973G>A	ENSP00000509289.1:p.Gly2325Ser
ENST00000693677.1:c.795-1G>A	ENSP00000509779.1:n.795-1G>A
ENST00000420124.4:c.7050-1G>A MANE Select	ENSP00000398837.2:n.7050-1G>A
ENST00000673918.1:c.6984-1G>A	ENSP00000501283.1:n.6984-1G>A
ENST00000674114.1:c.4372-1G>A
ENST00000420124.2:c.7050-1G>A	ENSP00000398837.1:n.7050-1G>A
ENST00000592092.1:n.430-1G>A
NM_014727.2:c.7050-1G>A	NP_055542.1:n.7050-1G>A
XM_011527561.1:c.6984-1G>A	XP_011525863.1:n.6984-1G>A
XM_011527562.1:c.7050-1G>A	XP_011525864.1:n.7050-1G>A
XM_011527563.1:c.6774-1G>A	XP_011525865.1:n.6774-1G>A
XM_011527561.2:c.6486-1G>A	XP_011525863.2:n.6486-1G>A
XM_011527562.2:c.7050-1G>A	XP_011525864.1:n.7050-1G>A
XM_017027544.1:c.6960-1G>A	XP_016883033.1:n.6960-1G>A
XM_017027545.1:c.6486-1G>A	XP_016883034.1:n.6486-1G>A
XM_017027546.1:c.4014-1G>A	XP_016883035.1:n.4014-1G>A
NM_014727.3:c.7050-1G>A MANE Select	NP_055542.1:n.7050-1G>A