Canonical Allele Identifier: CA405408563

Gene: KMT2B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35725088G>A , CM000681.2:g.35725088G>A	GRCh38
NC_000019.9:g.36215989G>A , CM000681.1:g.36215989G>A	GRCh37
NC_000019.8:g.40907829G>A	NCBI36
NG_052906.1:g.12070G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.3462+1G>A	ENSP00000501283.1:n.3462+1G>A
ENST00000674114.2:c.1069+1G>A	ENSP00000501039.2:n.1069+1G>A
ENST00000685609.1:c.99+1G>A	ENSP00000509152.1:n.99+1G>A
ENST00000691855.1:c.3070+1G>A
ENST00000691968.1:c.99+1G>A	ENSP00000508504.1:n.99+1G>A
ENST00000692961.1:c.3528+1G>A	ENSP00000509289.1:n.3528+1G>A
ENST00000693540.1:c.99+1G>A	ENSP00000509503.1:n.99+1G>A
ENST00000420124.4:c.3528+1G>A MANE Select	ENSP00000398837.2:n.3528+1G>A
ENST00000673918.1:c.3462+1G>A	ENSP00000501283.1:n.3462+1G>A
ENST00000674114.1:c.850+1G>A
ENST00000420124.2:c.3528+1G>A	ENSP00000398837.1:n.3528+1G>A
NM_014727.2:c.3528+1G>A	NP_055542.1:n.3528+1G>A
XM_011527561.1:c.3462+1G>A	XP_011525863.1:n.3462+1G>A
XM_011527562.1:c.3528+1G>A	XP_011525864.1:n.3528+1G>A
XM_011527563.1:c.3252+1G>A	XP_011525865.1:n.3252+1G>A
XR_935878.1:n.3552+1G>A
XM_011527561.2:c.2964+1G>A	XP_011525863.2:n.2964+1G>A
XM_011527562.2:c.3528+1G>A	XP_011525864.1:n.3528+1G>A
XM_017027544.1:c.3528+1G>A	XP_016883033.1:n.3528+1G>A
XM_017027545.1:c.2964+1G>A	XP_016883034.1:n.2964+1G>A
XM_017027546.1:c.492+1G>A	XP_016883035.1:n.492+1G>A
XR_935878.2:n.3729+1G>A
NM_014727.3:c.3528+1G>A MANE Select	NP_055542.1:n.3528+1G>A