Canonical Allele Identifier: CA2584575351

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35733697-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733697A>G , CM000681.2:g.35733697A>G	GRCh38
NC_000019.9:g.36224598A>G , CM000681.1:g.36224598A>G	GRCh37
NC_000019.8:g.40916438A>G	NCBI36
NG_052906.1:g.20679A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.1454A>G
ENST00000673918.2:c.6983+11A>G	ENSP00000501283.1:n.6983+11A>G
ENST00000674114.2:c.4590+11A>G	ENSP00000501039.2:n.4590+11A>G
ENST00000684977.1:c.2244+11A>G	ENSP00000509384.1:n.2244+11A>G
ENST00000689544.1:n.2290+11A>G
ENST00000691421.1:c.2181-66A>G	ENSP00000508674.1:n.2181-66A>G
ENST00000691855.1:c.6591+11A>G
ENST00000692961.1:c.6960-52A>G	ENSP00000509289.1:n.6960-52A>G
ENST00000693677.1:c.794+11A>G	ENSP00000509779.1:n.794+11A>G
ENST00000420124.4:c.7049+11A>G MANE Select	ENSP00000398837.2:n.7049+11A>G
ENST00000673918.1:c.6983+11A>G	ENSP00000501283.1:n.6983+11A>G
ENST00000674114.1:c.4371+11A>G
ENST00000420124.2:c.7049+11A>G	ENSP00000398837.1:n.7049+11A>G
ENST00000592092.1:n.429+11A>G
NM_014727.2:c.7049+11A>G	NP_055542.1:n.7049+11A>G
XM_011527561.1:c.6983+11A>G	XP_011525863.1:n.6983+11A>G
XM_011527562.1:c.7049+11A>G	XP_011525864.1:n.7049+11A>G
XM_011527563.1:c.6773+11A>G	XP_011525865.1:n.6773+11A>G
XM_011527561.2:c.6485+11A>G	XP_011525863.2:n.6485+11A>G
XM_011527562.2:c.7049+11A>G	XP_011525864.1:n.7049+11A>G
XM_017027544.1:c.6960-66A>G	XP_016883033.1:n.6960-66A>G
XM_017027545.1:c.6485+11A>G	XP_016883034.1:n.6485+11A>G
XM_017027546.1:c.4013+11A>G	XP_016883035.1:n.4013+11A>G
NM_014727.3:c.7049+11A>G MANE Select	NP_055542.1:n.7049+11A>G