Canonical Allele Identifier: CA9385594

Gene: KMT2B

Linked Data

• ClinVar Variation Id: 738380
• ClinVar RCV Id: RCV000914259 ; RCV004551803
• dbSNP Id: rs374561411
• ExAC: 19:36223501 C / T
• gnomAD v2: 19-36223501-C-T
• gnomAD v3: 19-35732600-C-T
• gnomAD v4: 19-35732600-C-T
• MyVariant Identifiers: chr19:g.36223501C>T (hg19) ; chr19:g.35732600C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732600C>T , CM000681.2:g.35732600C>T	GRCh38
NC_000019.9:g.36223501C>T , CM000681.1:g.36223501C>T	GRCh37
NC_000019.8:g.40915341C>T	NCBI36
NG_052906.1:g.19582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.357C>T
ENST00000673918.2:c.5985C>T	ENSP00000501283.1:p.His1995=
ENST00000674114.2:c.3592C>T	ENSP00000501039.2:n.3592C>T
ENST00000684977.1:c.1269C>T	ENSP00000509384.1:p.His423=
ENST00000689544.1:n.1204C>T
ENST00000691421.1:c.1272C>T	ENSP00000508674.1:p.His424=
ENST00000691855.1:c.5593C>T
ENST00000692961.1:c.6051C>T	ENSP00000509289.1:p.His2017=
ENST00000693677.1:c.704+271C>T	ENSP00000509779.1:n.704+271C>T
ENST00000420124.4:c.6051C>T MANE Select	ENSP00000398837.2:p.His2017=
ENST00000673918.1:c.5985C>T	ENSP00000501283.1:p.His1995=
ENST00000674114.1:c.3373C>T
ENST00000420124.2:c.6051C>T	ENSP00000398837.1:p.His2017=
NM_014727.2:c.6051C>T	NP_055542.1:p.His2017=
XM_011527561.1:c.5985C>T	XP_011525863.1:p.His1995=
XM_011527562.1:c.6051C>T	XP_011525864.1:p.His2017=
XM_011527563.1:c.5775C>T	XP_011525865.1:p.His1925=
XM_011527561.2:c.5487C>T	XP_011525863.2:p.His1829=
XM_011527562.2:c.6051C>T	XP_011525864.1:p.His2017=
XM_017027544.1:c.6051C>T	XP_016883033.1:p.His2017=
XM_017027545.1:c.5487C>T	XP_016883034.1:p.His1829=
XM_017027546.1:c.3015C>T	XP_016883035.1:p.His1005=
NM_014727.3:c.6051C>T MANE Select	NP_055542.1:p.His2017=