Canonical Allele Identifier: CA405429585

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224075G>A (hg19) ; chr19:g.35733174G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733174G>A , CM000681.2:g.35733174G>A	GRCh38
NC_000019.9:g.36224075G>A , CM000681.1:g.36224075G>A	GRCh37
NC_000019.8:g.40915915G>A	NCBI36
NG_052906.1:g.20156G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.931G>A
ENST00000673918.2:c.6559G>A	ENSP00000501283.1:p.Glu2187Lys
ENST00000674114.2:c.4166G>A	ENSP00000501039.2:n.4166G>A
ENST00000684977.1:c.1843G>A	ENSP00000509384.1:p.Glu615Lys
ENST00000689544.1:n.1778G>A
ENST00000691421.1:c.1846G>A	ENSP00000508674.1:p.Glu616Lys
ENST00000691855.1:c.6167G>A
ENST00000692961.1:c.6625G>A	ENSP00000509289.1:p.Glu2209Lys
ENST00000693677.1:c.705-423G>A	ENSP00000509779.1:n.705-423G>A
ENST00000420124.4:c.6625G>A MANE Select	ENSP00000398837.2:p.Glu2209Lys
ENST00000673918.1:c.6559G>A	ENSP00000501283.1:p.Glu2187Lys
ENST00000674114.1:c.3947G>A
ENST00000420124.2:c.6625G>A	ENSP00000398837.1:p.Glu2209Lys
NM_014727.2:c.6625G>A	NP_055542.1:p.Glu2209Lys
XM_011527561.1:c.6559G>A	XP_011525863.1:p.Glu2187Lys
XM_011527562.1:c.6625G>A	XP_011525864.1:p.Glu2209Lys
XM_011527563.1:c.6349G>A	XP_011525865.1:p.Glu2117Lys
XM_011527561.2:c.6061G>A	XP_011525863.2:p.Glu2021Lys
XM_011527562.2:c.6625G>A	XP_011525864.1:p.Glu2209Lys
XM_017027544.1:c.6625G>A	XP_016883033.1:p.Glu2209Lys
XM_017027545.1:c.6061G>A	XP_016883034.1:p.Glu2021Lys
XM_017027546.1:c.3589G>A	XP_016883035.1:p.Glu1197Lys
NM_014727.3:c.6625G>A MANE Select	NP_055542.1:p.Glu2209Lys