Canonical Allele Identifier: CA405429747

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224109T>G (hg19) ; chr19:g.35733208T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733208T>G , CM000681.2:g.35733208T>G	GRCh38
NC_000019.9:g.36224109T>G , CM000681.1:g.36224109T>G	GRCh37
NC_000019.8:g.40915949T>G	NCBI36
NG_052906.1:g.20190T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.965T>G
ENST00000673918.2:c.6593T>G	ENSP00000501283.1:p.Leu2198Trp
ENST00000674114.2:c.4200T>G	ENSP00000501039.2:n.4200T>G
ENST00000684977.1:c.1877T>G	ENSP00000509384.1:p.Leu626Trp
ENST00000689544.1:n.1812T>G
ENST00000691421.1:c.1880T>G	ENSP00000508674.1:p.Leu627Trp
ENST00000691855.1:c.6201T>G
ENST00000692961.1:c.6659T>G	ENSP00000509289.1:p.Leu2220Trp
ENST00000693677.1:c.705-389T>G	ENSP00000509779.1:n.705-389T>G
ENST00000420124.4:c.6659T>G MANE Select	ENSP00000398837.2:p.Leu2220Trp
ENST00000673918.1:c.6593T>G	ENSP00000501283.1:p.Leu2198Trp
ENST00000674114.1:c.3981T>G
ENST00000420124.2:c.6659T>G	ENSP00000398837.1:p.Leu2220Trp
NM_014727.2:c.6659T>G	NP_055542.1:p.Leu2220Trp
XM_011527561.1:c.6593T>G	XP_011525863.1:p.Leu2198Trp
XM_011527562.1:c.6659T>G	XP_011525864.1:p.Leu2220Trp
XM_011527563.1:c.6383T>G	XP_011525865.1:p.Leu2128Trp
XM_011527561.2:c.6095T>G	XP_011525863.2:p.Leu2032Trp
XM_011527562.2:c.6659T>G	XP_011525864.1:p.Leu2220Trp
XM_017027544.1:c.6659T>G	XP_016883033.1:p.Leu2220Trp
XM_017027545.1:c.6095T>G	XP_016883034.1:p.Leu2032Trp
XM_017027546.1:c.3623T>G	XP_016883035.1:p.Leu1208Trp
NM_014727.3:c.6659T>G MANE Select	NP_055542.1:p.Leu2220Trp