Canonical Allele Identifier: CA405419351

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36221020T>G (hg19) ; chr19:g.35730119T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730119T>G , CM000681.2:g.35730119T>G	GRCh38
NC_000019.9:g.36221020T>G , CM000681.1:g.36221020T>G	GRCh37
NC_000019.8:g.40912860T>G	NCBI36
NG_052906.1:g.17101T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.5004T>G	ENSP00000501283.1:p.Asp1668Glu
ENST00000674114.2:c.2611T>G	ENSP00000501039.2:n.2611T>G
ENST00000684977.1:c.288T>G	ENSP00000509384.1:p.Asp96Glu
ENST00000685168.1:c.496T>G
ENST00000689544.1:n.223T>G
ENST00000691421.1:c.291T>G	ENSP00000508674.1:p.Asp97Glu
ENST00000691855.1:c.4612T>G
ENST00000692961.1:c.5070T>G	ENSP00000509289.1:p.Asp1690Glu
ENST00000420124.4:c.5070T>G MANE Select	ENSP00000398837.2:p.Asp1690Glu
ENST00000673918.1:c.5004T>G	ENSP00000501283.1:p.Asp1668Glu
ENST00000674114.1:c.2392T>G
ENST00000420124.2:c.5070T>G	ENSP00000398837.1:p.Asp1690Glu
NM_014727.2:c.5070T>G	NP_055542.1:p.Asp1690Glu
XM_011527561.1:c.5004T>G	XP_011525863.1:p.Asp1668Glu
XM_011527562.1:c.5070T>G	XP_011525864.1:p.Asp1690Glu
XM_011527563.1:c.4794T>G	XP_011525865.1:p.Asp1598Glu
XM_011527561.2:c.4506T>G	XP_011525863.2:p.Asp1502Glu
XM_011527562.2:c.5070T>G	XP_011525864.1:p.Asp1690Glu
XM_017027544.1:c.5070T>G	XP_016883033.1:p.Asp1690Glu
XM_017027545.1:c.4506T>G	XP_016883034.1:p.Asp1502Glu
XM_017027546.1:c.2034T>G	XP_016883035.1:p.Asp678Glu
NM_014727.3:c.5070T>G MANE Select	NP_055542.1:p.Asp1690Glu