Canonical Allele Identifier: CA405419345

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36221018G>C (hg19) ; chr19:g.35730117G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730117G>C , CM000681.2:g.35730117G>C	GRCh38
NC_000019.9:g.36221018G>C , CM000681.1:g.36221018G>C	GRCh37
NC_000019.8:g.40912858G>C	NCBI36
NG_052906.1:g.17099G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.5002G>C	ENSP00000501283.1:p.Asp1668His
ENST00000674114.2:c.2609G>C	ENSP00000501039.2:n.2609G>C
ENST00000684977.1:c.286G>C	ENSP00000509384.1:p.Asp96His
ENST00000685168.1:c.494G>C
ENST00000689544.1:n.221G>C
ENST00000691421.1:c.289G>C	ENSP00000508674.1:p.Asp97His
ENST00000691855.1:c.4610G>C
ENST00000692961.1:c.5068G>C	ENSP00000509289.1:p.Asp1690His
ENST00000420124.4:c.5068G>C MANE Select	ENSP00000398837.2:p.Asp1690His
ENST00000673918.1:c.5002G>C	ENSP00000501283.1:p.Asp1668His
ENST00000674114.1:c.2390G>C
ENST00000420124.2:c.5068G>C	ENSP00000398837.1:p.Asp1690His
NM_014727.2:c.5068G>C	NP_055542.1:p.Asp1690His
XM_011527561.1:c.5002G>C	XP_011525863.1:p.Asp1668His
XM_011527562.1:c.5068G>C	XP_011525864.1:p.Asp1690His
XM_011527563.1:c.4792G>C	XP_011525865.1:p.Asp1598His
XM_011527561.2:c.4504G>C	XP_011525863.2:p.Asp1502His
XM_011527562.2:c.5068G>C	XP_011525864.1:p.Asp1690His
XM_017027544.1:c.5068G>C	XP_016883033.1:p.Asp1690His
XM_017027545.1:c.4504G>C	XP_016883034.1:p.Asp1502His
XM_017027546.1:c.2032G>C	XP_016883035.1:p.Asp678His
NM_014727.3:c.5068G>C MANE Select	NP_055542.1:p.Asp1690His