Canonical Allele Identifier: CA405424637

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223384G>C (hg19) ; chr19:g.35732483G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732483G>C , CM000681.2:g.35732483G>C	GRCh38
NC_000019.9:g.36223384G>C , CM000681.1:g.36223384G>C	GRCh37
NC_000019.8:g.40915224G>C	NCBI36
NG_052906.1:g.19465G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.240G>C
ENST00000673918.2:c.5868G>C	ENSP00000501283.1:p.Glu1956Asp
ENST00000674114.2:c.3475G>C	ENSP00000501039.2:n.3475G>C
ENST00000684977.1:c.1152G>C	ENSP00000509384.1:p.Glu384Asp
ENST00000689544.1:n.1087G>C
ENST00000691421.1:c.1155G>C	ENSP00000508674.1:p.Glu385Asp
ENST00000691855.1:c.5476G>C
ENST00000692961.1:c.5934G>C	ENSP00000509289.1:p.Glu1978Asp
ENST00000693677.1:c.704+154G>C	ENSP00000509779.1:n.704+154G>C
ENST00000420124.4:c.5934G>C MANE Select	ENSP00000398837.2:p.Glu1978Asp
ENST00000673918.1:c.5868G>C	ENSP00000501283.1:p.Glu1956Asp
ENST00000674114.1:c.3256G>C
ENST00000420124.2:c.5934G>C	ENSP00000398837.1:p.Glu1978Asp
NM_014727.2:c.5934G>C	NP_055542.1:p.Glu1978Asp
XM_011527561.1:c.5868G>C	XP_011525863.1:p.Glu1956Asp
XM_011527562.1:c.5934G>C	XP_011525864.1:p.Glu1978Asp
XM_011527563.1:c.5658G>C	XP_011525865.1:p.Glu1886Asp
XM_011527561.2:c.5370G>C	XP_011525863.2:p.Glu1790Asp
XM_011527562.2:c.5934G>C	XP_011525864.1:p.Glu1978Asp
XM_017027544.1:c.5934G>C	XP_016883033.1:p.Glu1978Asp
XM_017027545.1:c.5370G>C	XP_016883034.1:p.Glu1790Asp
XM_017027546.1:c.2898G>C	XP_016883035.1:p.Glu966Asp
NM_014727.3:c.5934G>C MANE Select	NP_055542.1:p.Glu1978Asp