Canonical Allele Identifier: CA405419323

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36221007C>A (hg19) ; chr19:g.35730106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730106C>A , CM000681.2:g.35730106C>A	GRCh38
NC_000019.9:g.36221007C>A , CM000681.1:g.36221007C>A	GRCh37
NC_000019.8:g.40912847C>A	NCBI36
NG_052906.1:g.17088C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4991C>A	ENSP00000501283.1:p.Thr1664Asn
ENST00000674114.2:c.2598C>A	ENSP00000501039.2:n.2598C>A
ENST00000684977.1:c.275C>A	ENSP00000509384.1:p.Thr92Asn
ENST00000685168.1:c.483C>A
ENST00000689544.1:n.210C>A
ENST00000691421.1:c.278C>A	ENSP00000508674.1:p.Thr93Asn
ENST00000691855.1:c.4599C>A
ENST00000692961.1:c.5057C>A	ENSP00000509289.1:p.Thr1686Asn
ENST00000420124.4:c.5057C>A MANE Select	ENSP00000398837.2:p.Thr1686Asn
ENST00000673918.1:c.4991C>A	ENSP00000501283.1:p.Thr1664Asn
ENST00000674114.1:c.2379C>A
ENST00000420124.2:c.5057C>A	ENSP00000398837.1:p.Thr1686Asn
NM_014727.2:c.5057C>A	NP_055542.1:p.Thr1686Asn
XM_011527561.1:c.4991C>A	XP_011525863.1:p.Thr1664Asn
XM_011527562.1:c.5057C>A	XP_011525864.1:p.Thr1686Asn
XM_011527563.1:c.4781C>A	XP_011525865.1:p.Thr1594Asn
XM_011527561.2:c.4493C>A	XP_011525863.2:p.Thr1498Asn
XM_011527562.2:c.5057C>A	XP_011525864.1:p.Thr1686Asn
XM_017027544.1:c.5057C>A	XP_016883033.1:p.Thr1686Asn
XM_017027545.1:c.4493C>A	XP_016883034.1:p.Thr1498Asn
XM_017027546.1:c.2021C>A	XP_016883035.1:p.Thr674Asn
NM_014727.3:c.5057C>A MANE Select	NP_055542.1:p.Thr1686Asn