Canonical Allele Identifier: CA405418669

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220875A>G (hg19) ; chr19:g.35729974A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729974A>G , CM000681.2:g.35729974A>G	GRCh38
NC_000019.9:g.36220875A>G , CM000681.1:g.36220875A>G	GRCh37
NC_000019.8:g.40912715A>G	NCBI36
NG_052906.1:g.16956A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4859A>G	ENSP00000501283.1:p.Glu1620Gly
ENST00000674114.2:c.2466A>G	ENSP00000501039.2:n.2466A>G
ENST00000684977.1:c.143A>G	ENSP00000509384.1:p.Glu48Gly
ENST00000685168.1:c.351A>G
ENST00000689544.1:n.78A>G
ENST00000691421.1:c.146A>G	ENSP00000508674.1:p.Glu49Gly
ENST00000691855.1:c.4467A>G
ENST00000692961.1:c.4925A>G	ENSP00000509289.1:p.Glu1642Gly
ENST00000420124.4:c.4925A>G MANE Select	ENSP00000398837.2:p.Glu1642Gly
ENST00000673918.1:c.4859A>G	ENSP00000501283.1:p.Glu1620Gly
ENST00000674114.1:c.2247A>G
ENST00000420124.2:c.4925A>G	ENSP00000398837.1:p.Glu1642Gly
NM_014727.2:c.4925A>G	NP_055542.1:p.Glu1642Gly
XM_011527561.1:c.4859A>G	XP_011525863.1:p.Glu1620Gly
XM_011527562.1:c.4925A>G	XP_011525864.1:p.Glu1642Gly
XM_011527563.1:c.4649A>G	XP_011525865.1:p.Glu1550Gly
XM_011527561.2:c.4361A>G	XP_011525863.2:p.Glu1454Gly
XM_011527562.2:c.4925A>G	XP_011525864.1:p.Glu1642Gly
XM_017027544.1:c.4925A>G	XP_016883033.1:p.Glu1642Gly
XM_017027545.1:c.4361A>G	XP_016883034.1:p.Glu1454Gly
XM_017027546.1:c.1889A>G	XP_016883035.1:p.Glu630Gly
NM_014727.3:c.4925A>G MANE Select	NP_055542.1:p.Glu1642Gly