Canonical Allele Identifier: CA405419312

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36221003C>A (hg19) ; chr19:g.35730102C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730102C>A , CM000681.2:g.35730102C>A	GRCh38
NC_000019.9:g.36221003C>A , CM000681.1:g.36221003C>A	GRCh37
NC_000019.8:g.40912843C>A	NCBI36
NG_052906.1:g.17084C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4987C>A	ENSP00000501283.1:p.His1663Asn
ENST00000674114.2:c.2594C>A	ENSP00000501039.2:n.2594C>A
ENST00000684977.1:c.271C>A	ENSP00000509384.1:p.His91Asn
ENST00000685168.1:c.479C>A
ENST00000689544.1:n.206C>A
ENST00000691421.1:c.274C>A	ENSP00000508674.1:p.His92Asn
ENST00000691855.1:c.4595C>A
ENST00000692961.1:c.5053C>A	ENSP00000509289.1:p.His1685Asn
ENST00000420124.4:c.5053C>A MANE Select	ENSP00000398837.2:p.His1685Asn
ENST00000673918.1:c.4987C>A	ENSP00000501283.1:p.His1663Asn
ENST00000674114.1:c.2375C>A
ENST00000420124.2:c.5053C>A	ENSP00000398837.1:p.His1685Asn
NM_014727.2:c.5053C>A	NP_055542.1:p.His1685Asn
XM_011527561.1:c.4987C>A	XP_011525863.1:p.His1663Asn
XM_011527562.1:c.5053C>A	XP_011525864.1:p.His1685Asn
XM_011527563.1:c.4777C>A	XP_011525865.1:p.His1593Asn
XM_011527561.2:c.4489C>A	XP_011525863.2:p.His1497Asn
XM_011527562.2:c.5053C>A	XP_011525864.1:p.His1685Asn
XM_017027544.1:c.5053C>A	XP_016883033.1:p.His1685Asn
XM_017027545.1:c.4489C>A	XP_016883034.1:p.His1497Asn
XM_017027546.1:c.2017C>A	XP_016883035.1:p.His673Asn
NM_014727.3:c.5053C>A MANE Select	NP_055542.1:p.His1685Asn