Canonical Allele Identifier: CA405419326

Gene: KMT2B

Linked Data

• COSMIC: COSM418318
• MyVariant Identifiers: chr19:g.36221009G>A (hg19) ; chr19:g.35730108G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730108G>A , CM000681.2:g.35730108G>A	GRCh38
NC_000019.9:g.36221009G>A , CM000681.1:g.36221009G>A	GRCh37
NC_000019.8:g.40912849G>A	NCBI36
NG_052906.1:g.17090G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4993G>A	ENSP00000501283.1:p.Asp1665Asn
ENST00000674114.2:c.2600G>A	ENSP00000501039.2:n.2600G>A
ENST00000684977.1:c.277G>A	ENSP00000509384.1:p.Asp93Asn
ENST00000685168.1:c.485G>A
ENST00000689544.1:n.212G>A
ENST00000691421.1:c.280G>A	ENSP00000508674.1:p.Asp94Asn
ENST00000691855.1:c.4601G>A
ENST00000692961.1:c.5059G>A	ENSP00000509289.1:p.Asp1687Asn
ENST00000420124.4:c.5059G>A MANE Select	ENSP00000398837.2:p.Asp1687Asn
ENST00000673918.1:c.4993G>A	ENSP00000501283.1:p.Asp1665Asn
ENST00000674114.1:c.2381G>A
ENST00000420124.2:c.5059G>A	ENSP00000398837.1:p.Asp1687Asn
NM_014727.2:c.5059G>A	NP_055542.1:p.Asp1687Asn
XM_011527561.1:c.4993G>A	XP_011525863.1:p.Asp1665Asn
XM_011527562.1:c.5059G>A	XP_011525864.1:p.Asp1687Asn
XM_011527563.1:c.4783G>A	XP_011525865.1:p.Asp1595Asn
XM_011527561.2:c.4495G>A	XP_011525863.2:p.Asp1499Asn
XM_011527562.2:c.5059G>A	XP_011525864.1:p.Asp1687Asn
XM_017027544.1:c.5059G>A	XP_016883033.1:p.Asp1687Asn
XM_017027545.1:c.4495G>A	XP_016883034.1:p.Asp1499Asn
XM_017027546.1:c.2023G>A	XP_016883035.1:p.Asp675Asn
NM_014727.3:c.5059G>A MANE Select	NP_055542.1:p.Asp1687Asn