Canonical Allele Identifier: CA405419219

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220981C>A (hg19) ; chr19:g.35730080C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730080C>A , CM000681.2:g.35730080C>A	GRCh38
NC_000019.9:g.36220981C>A , CM000681.1:g.36220981C>A	GRCh37
NC_000019.8:g.40912821C>A	NCBI36
NG_052906.1:g.17062C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4965C>A	ENSP00000501283.1:p.Asp1655Glu
ENST00000674114.2:c.2572C>A	ENSP00000501039.2:n.2572C>A
ENST00000684977.1:c.249C>A	ENSP00000509384.1:p.Asp83Glu
ENST00000685168.1:c.457C>A
ENST00000689544.1:n.184C>A
ENST00000691421.1:c.252C>A	ENSP00000508674.1:p.Asp84Glu
ENST00000691855.1:c.4573C>A
ENST00000692961.1:c.5031C>A	ENSP00000509289.1:p.Asp1677Glu
ENST00000420124.4:c.5031C>A MANE Select	ENSP00000398837.2:p.Asp1677Glu
ENST00000673918.1:c.4965C>A	ENSP00000501283.1:p.Asp1655Glu
ENST00000674114.1:c.2353C>A
ENST00000420124.2:c.5031C>A	ENSP00000398837.1:p.Asp1677Glu
NM_014727.2:c.5031C>A	NP_055542.1:p.Asp1677Glu
XM_011527561.1:c.4965C>A	XP_011525863.1:p.Asp1655Glu
XM_011527562.1:c.5031C>A	XP_011525864.1:p.Asp1677Glu
XM_011527563.1:c.4755C>A	XP_011525865.1:p.Asp1585Glu
XM_011527561.2:c.4467C>A	XP_011525863.2:p.Asp1489Glu
XM_011527562.2:c.5031C>A	XP_011525864.1:p.Asp1677Glu
XM_017027544.1:c.5031C>A	XP_016883033.1:p.Asp1677Glu
XM_017027545.1:c.4467C>A	XP_016883034.1:p.Asp1489Glu
XM_017027546.1:c.1995C>A	XP_016883035.1:p.Asp665Glu
NM_014727.3:c.5031C>A MANE Select	NP_055542.1:p.Asp1677Glu