Canonical Allele Identifier: CA405379391

Gene: KMT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35719939C>T , CM000681.2:g.35719939C>T	GRCh38
NC_000019.9:g.36210841C>T , CM000681.1:g.36210841C>T	GRCh37
NC_000019.8:g.40902681C>T	NCBI36
NG_052906.1:g.6921C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014727.3:c.592C>T MANE Select	NP_055542.1:p.Arg198Trp
ENST00000420124.4:c.592C>T MANE Select	ENSP00000398837.2:p.Arg198Trp
NM_014727.2:c.592C>T	NP_055542.1:p.Arg198Trp
ENST00000420124.2:c.592C>T	ENSP00000398837.1:p.Arg198Trp
ENST00000673918.1:c.526C>T	ENSP00000501283.1:p.Arg176Trp
ENST00000673918.2:c.526C>T	ENSP00000501283.1:p.Arg176Trp
ENST00000687718.1:c.*93C>T	ENSP00000510535.1:n.*93C>T
ENST00000689139.1:c.90C>T
ENST00000691855.1:c.90C>T
ENST00000692961.1:c.592C>T	ENSP00000509289.1:p.Arg198Trp
XM_011527561.1:c.526C>T	XP_011525863.1:p.Arg176Trp
XM_011527561.2:c.28C>T	XP_011525863.2:p.Arg10Trp
XM_011527562.1:c.592C>T	XP_011525864.1:p.Arg198Trp
XM_011527562.2:c.592C>T	XP_011525864.1:p.Arg198Trp
XM_011527563.1:c.592C>T	XP_011525865.1:p.Arg198Trp
XM_017027544.1:c.592C>T	XP_016883033.1:p.Arg198Trp
XM_017027545.1:c.28C>T	XP_016883034.1:p.Arg10Trp
XR_935878.1:n.616C>T
XR_935878.2:n.793C>T