Canonical Allele Identifier: CA405419214

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220980A>G (hg19) ; chr19:g.35730079A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730079A>G , CM000681.2:g.35730079A>G	GRCh38
NC_000019.9:g.36220980A>G , CM000681.1:g.36220980A>G	GRCh37
NC_000019.8:g.40912820A>G	NCBI36
NG_052906.1:g.17061A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4964A>G	ENSP00000501283.1:p.Asp1655Gly
ENST00000674114.2:c.2571A>G	ENSP00000501039.2:n.2571A>G
ENST00000684977.1:c.248A>G	ENSP00000509384.1:p.Asp83Gly
ENST00000685168.1:c.456A>G
ENST00000689544.1:n.183A>G
ENST00000691421.1:c.251A>G	ENSP00000508674.1:p.Asp84Gly
ENST00000691855.1:c.4572A>G
ENST00000692961.1:c.5030A>G	ENSP00000509289.1:p.Asp1677Gly
ENST00000420124.4:c.5030A>G MANE Select	ENSP00000398837.2:p.Asp1677Gly
ENST00000673918.1:c.4964A>G	ENSP00000501283.1:p.Asp1655Gly
ENST00000674114.1:c.2352A>G
ENST00000420124.2:c.5030A>G	ENSP00000398837.1:p.Asp1677Gly
NM_014727.2:c.5030A>G	NP_055542.1:p.Asp1677Gly
XM_011527561.1:c.4964A>G	XP_011525863.1:p.Asp1655Gly
XM_011527562.1:c.5030A>G	XP_011525864.1:p.Asp1677Gly
XM_011527563.1:c.4754A>G	XP_011525865.1:p.Asp1585Gly
XM_011527561.2:c.4466A>G	XP_011525863.2:p.Asp1489Gly
XM_011527562.2:c.5030A>G	XP_011525864.1:p.Asp1677Gly
XM_017027544.1:c.5030A>G	XP_016883033.1:p.Asp1677Gly
XM_017027545.1:c.4466A>G	XP_016883034.1:p.Asp1489Gly
XM_017027546.1:c.1994A>G	XP_016883035.1:p.Asp665Gly
NM_014727.3:c.5030A>G MANE Select	NP_055542.1:p.Asp1677Gly