Canonical Allele Identifier: CA405424533

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732463-G-A
• MyVariant Identifiers: chr19:g.36223364G>A (hg19) ; chr19:g.35732463G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732463G>A , CM000681.2:g.35732463G>A	GRCh38
NC_000019.9:g.36223364G>A , CM000681.1:g.36223364G>A	GRCh37
NC_000019.8:g.40915204G>A	NCBI36
NG_052906.1:g.19445G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.220G>A
ENST00000673918.2:c.5848G>A	ENSP00000501283.1:p.Asp1950Asn
ENST00000674114.2:c.3455G>A	ENSP00000501039.2:n.3455G>A
ENST00000684977.1:c.1132G>A	ENSP00000509384.1:p.Asp378Asn
ENST00000689544.1:n.1067G>A
ENST00000691421.1:c.1135G>A	ENSP00000508674.1:p.Asp379Asn
ENST00000691855.1:c.5456G>A
ENST00000692961.1:c.5914G>A	ENSP00000509289.1:p.Asp1972Asn
ENST00000693677.1:c.704+134G>A	ENSP00000509779.1:n.704+134G>A
ENST00000420124.4:c.5914G>A MANE Select	ENSP00000398837.2:p.Asp1972Asn
ENST00000673918.1:c.5848G>A	ENSP00000501283.1:p.Asp1950Asn
ENST00000674114.1:c.3236G>A
ENST00000420124.2:c.5914G>A	ENSP00000398837.1:p.Asp1972Asn
NM_014727.2:c.5914G>A	NP_055542.1:p.Asp1972Asn
XM_011527561.1:c.5848G>A	XP_011525863.1:p.Asp1950Asn
XM_011527562.1:c.5914G>A	XP_011525864.1:p.Asp1972Asn
XM_011527563.1:c.5638G>A	XP_011525865.1:p.Asp1880Asn
XM_011527561.2:c.5350G>A	XP_011525863.2:p.Asp1784Asn
XM_011527562.2:c.5914G>A	XP_011525864.1:p.Asp1972Asn
XM_017027544.1:c.5914G>A	XP_016883033.1:p.Asp1972Asn
XM_017027545.1:c.5350G>A	XP_016883034.1:p.Asp1784Asn
XM_017027546.1:c.2878G>A	XP_016883035.1:p.Asp960Asn
NM_014727.3:c.5914G>A MANE Select	NP_055542.1:p.Asp1972Asn