Canonical Allele Identifier: CA405419038

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220952C>G (hg19) ; chr19:g.35730051C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730051C>G , CM000681.2:g.35730051C>G	GRCh38
NC_000019.9:g.36220952C>G , CM000681.1:g.36220952C>G	GRCh37
NC_000019.8:g.40912792C>G	NCBI36
NG_052906.1:g.17033C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000673918.2:c.4936C>G	ENSP00000501283.1:p.Arg1646Gly
ENST00000674114.2:c.2543C>G	ENSP00000501039.2:n.2543C>G
ENST00000684977.1:c.220C>G	ENSP00000509384.1:p.Arg74Gly
ENST00000685168.1:c.428C>G
ENST00000689544.1:n.155C>G
ENST00000691421.1:c.223C>G	ENSP00000508674.1:p.Arg75Gly
ENST00000691855.1:c.4544C>G
ENST00000692961.1:c.5002C>G	ENSP00000509289.1:p.Arg1668Gly
ENST00000420124.4:c.5002C>G MANE Select	ENSP00000398837.2:p.Arg1668Gly
ENST00000673918.1:c.4936C>G	ENSP00000501283.1:p.Arg1646Gly
ENST00000674114.1:c.2324C>G
ENST00000420124.2:c.5002C>G	ENSP00000398837.1:p.Arg1668Gly
NM_014727.2:c.5002C>G	NP_055542.1:p.Arg1668Gly
XM_011527561.1:c.4936C>G	XP_011525863.1:p.Arg1646Gly
XM_011527562.1:c.5002C>G	XP_011525864.1:p.Arg1668Gly
XM_011527563.1:c.4726C>G	XP_011525865.1:p.Arg1576Gly
XM_011527561.2:c.4438C>G	XP_011525863.2:p.Arg1480Gly
XM_011527562.2:c.5002C>G	XP_011525864.1:p.Arg1668Gly
XM_017027544.1:c.5002C>G	XP_016883033.1:p.Arg1668Gly
XM_017027545.1:c.4438C>G	XP_016883034.1:p.Arg1480Gly
XM_017027546.1:c.1966C>G	XP_016883035.1:p.Arg656Gly
NM_014727.3:c.5002C>G MANE Select	NP_055542.1:p.Arg1668Gly