Canonical Allele Identifier: CA405431529

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224675A>G (hg19) ; chr19:g.35733774A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733774A>G , CM000681.2:g.35733774A>G	GRCh38
NC_000019.9:g.36224675A>G , CM000681.1:g.36224675A>G	GRCh37
NC_000019.8:g.40916515A>G	NCBI36
NG_052906.1:g.20756A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.1531A>G
ENST00000673918.2:c.6995A>G	ENSP00000501283.1:p.Glu2332Gly
ENST00000674114.2:c.4602A>G	ENSP00000501039.2:n.4602A>G
ENST00000684977.1:c.2256A>G	ENSP00000509384.1:n.2256A>G
ENST00000689544.1:n.2302A>G
ENST00000689929.1:c.12A>G
ENST00000691421.1:c.2192A>G	ENSP00000508674.1:p.Glu731Gly
ENST00000691855.1:c.6603A>G
ENST00000692961.1:c.6985A>G	ENSP00000509289.1:p.Asn2329Asp
ENST00000693175.1:c.12A>G
ENST00000693677.1:c.806A>G	ENSP00000509779.1:p.Glu269Gly
ENST00000420124.4:c.7061A>G MANE Select	ENSP00000398837.2:p.Glu2354Gly
ENST00000673918.1:c.6995A>G	ENSP00000501283.1:p.Glu2332Gly
ENST00000674114.1:c.4383A>G
ENST00000420124.2:c.7061A>G	ENSP00000398837.1:p.Glu2354Gly
ENST00000592092.1:n.441A>G
NM_014727.2:c.7061A>G	NP_055542.1:p.Glu2354Gly
XM_011527561.1:c.6995A>G	XP_011525863.1:p.Glu2332Gly
XM_011527562.1:c.7061A>G	XP_011525864.1:p.Glu2354Gly
XM_011527563.1:c.6785A>G	XP_011525865.1:p.Glu2262Gly
XM_011527561.2:c.6497A>G	XP_011525863.2:p.Glu2166Gly
XM_011527562.2:c.7061A>G	XP_011525864.1:p.Glu2354Gly
XM_017027544.1:c.6971A>G	XP_016883033.1:p.Glu2324Gly
XM_017027545.1:c.6497A>G	XP_016883034.1:p.Glu2166Gly
XM_017027546.1:c.4025A>G	XP_016883035.1:p.Glu1342Gly
NM_014727.3:c.7061A>G MANE Select	NP_055542.1:p.Glu2354Gly