Canonical Allele Identifier: CA405427719

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223766C>A (hg19) ; chr19:g.35732865C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732865C>A , CM000681.2:g.35732865C>A	GRCh38
NC_000019.9:g.36223766C>A , CM000681.1:g.36223766C>A	GRCh37
NC_000019.8:g.40915606C>A	NCBI36
NG_052906.1:g.19847C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.622C>A
ENST00000673918.2:c.6250C>A	ENSP00000501283.1:p.Pro2084Thr
ENST00000674114.2:c.3857C>A	ENSP00000501039.2:n.3857C>A
ENST00000684977.1:c.1534C>A	ENSP00000509384.1:p.Pro512Thr
ENST00000689544.1:n.1469C>A
ENST00000691421.1:c.1537C>A	ENSP00000508674.1:p.Pro513Thr
ENST00000691855.1:c.5858C>A
ENST00000692961.1:c.6316C>A	ENSP00000509289.1:p.Pro2106Thr
ENST00000693677.1:c.704+536C>A	ENSP00000509779.1:n.704+536C>A
ENST00000420124.4:c.6316C>A MANE Select	ENSP00000398837.2:p.Pro2106Thr
ENST00000673918.1:c.6250C>A	ENSP00000501283.1:p.Pro2084Thr
ENST00000674114.1:c.3638C>A
ENST00000420124.2:c.6316C>A	ENSP00000398837.1:p.Pro2106Thr
NM_014727.2:c.6316C>A	NP_055542.1:p.Pro2106Thr
XM_011527561.1:c.6250C>A	XP_011525863.1:p.Pro2084Thr
XM_011527562.1:c.6316C>A	XP_011525864.1:p.Pro2106Thr
XM_011527563.1:c.6040C>A	XP_011525865.1:p.Pro2014Thr
XM_011527561.2:c.5752C>A	XP_011525863.2:p.Pro1918Thr
XM_011527562.2:c.6316C>A	XP_011525864.1:p.Pro2106Thr
XM_017027544.1:c.6316C>A	XP_016883033.1:p.Pro2106Thr
XM_017027545.1:c.5752C>A	XP_016883034.1:p.Pro1918Thr
XM_017027546.1:c.3280C>A	XP_016883035.1:p.Pro1094Thr
NM_014727.3:c.6316C>A MANE Select	NP_055542.1:p.Pro2106Thr