Canonical Allele Identifier: CA405424546

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223365A>T (hg19) ; chr19:g.35732464A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732464A>T , CM000681.2:g.35732464A>T	GRCh38
NC_000019.9:g.36223365A>T , CM000681.1:g.36223365A>T	GRCh37
NC_000019.8:g.40915205A>T	NCBI36
NG_052906.1:g.19446A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.221A>T
ENST00000673918.2:c.5849A>T	ENSP00000501283.1:p.Asp1950Val
ENST00000674114.2:c.3456A>T	ENSP00000501039.2:n.3456A>T
ENST00000684977.1:c.1133A>T	ENSP00000509384.1:p.Asp378Val
ENST00000689544.1:n.1068A>T
ENST00000691421.1:c.1136A>T	ENSP00000508674.1:p.Asp379Val
ENST00000691855.1:c.5457A>T
ENST00000692961.1:c.5915A>T	ENSP00000509289.1:p.Asp1972Val
ENST00000693677.1:c.704+135A>T	ENSP00000509779.1:n.704+135A>T
ENST00000420124.4:c.5915A>T MANE Select	ENSP00000398837.2:p.Asp1972Val
ENST00000673918.1:c.5849A>T	ENSP00000501283.1:p.Asp1950Val
ENST00000674114.1:c.3237A>T
ENST00000420124.2:c.5915A>T	ENSP00000398837.1:p.Asp1972Val
NM_014727.2:c.5915A>T	NP_055542.1:p.Asp1972Val
XM_011527561.1:c.5849A>T	XP_011525863.1:p.Asp1950Val
XM_011527562.1:c.5915A>T	XP_011525864.1:p.Asp1972Val
XM_011527563.1:c.5639A>T	XP_011525865.1:p.Asp1880Val
XM_011527561.2:c.5351A>T	XP_011525863.2:p.Asp1784Val
XM_011527562.2:c.5915A>T	XP_011525864.1:p.Asp1972Val
XM_017027544.1:c.5915A>T	XP_016883033.1:p.Asp1972Val
XM_017027545.1:c.5351A>T	XP_016883034.1:p.Asp1784Val
XM_017027546.1:c.2879A>T	XP_016883035.1:p.Asp960Val
NM_014727.3:c.5915A>T MANE Select	NP_055542.1:p.Asp1972Val