Canonical Allele Identifier: CA405427917

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223794A>C (hg19) ; chr19:g.35732893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732893A>C , CM000681.2:g.35732893A>C	GRCh38
NC_000019.9:g.36223794A>C , CM000681.1:g.36223794A>C	GRCh37
NC_000019.8:g.40915634A>C	NCBI36
NG_052906.1:g.19875A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.650A>C
ENST00000673918.2:c.6278A>C	ENSP00000501283.1:p.Asp2093Ala
ENST00000674114.2:c.3885A>C	ENSP00000501039.2:n.3885A>C
ENST00000684977.1:c.1562A>C	ENSP00000509384.1:p.Asp521Ala
ENST00000689544.1:n.1497A>C
ENST00000691421.1:c.1565A>C	ENSP00000508674.1:p.Asp522Ala
ENST00000691855.1:c.5886A>C
ENST00000692961.1:c.6344A>C	ENSP00000509289.1:p.Asp2115Ala
ENST00000693677.1:c.704+564A>C	ENSP00000509779.1:n.704+564A>C
ENST00000420124.4:c.6344A>C MANE Select	ENSP00000398837.2:p.Asp2115Ala
ENST00000673918.1:c.6278A>C	ENSP00000501283.1:p.Asp2093Ala
ENST00000674114.1:c.3666A>C
ENST00000420124.2:c.6344A>C	ENSP00000398837.1:p.Asp2115Ala
NM_014727.2:c.6344A>C	NP_055542.1:p.Asp2115Ala
XM_011527561.1:c.6278A>C	XP_011525863.1:p.Asp2093Ala
XM_011527562.1:c.6344A>C	XP_011525864.1:p.Asp2115Ala
XM_011527563.1:c.6068A>C	XP_011525865.1:p.Asp2023Ala
XM_011527561.2:c.5780A>C	XP_011525863.2:p.Asp1927Ala
XM_011527562.2:c.6344A>C	XP_011525864.1:p.Asp2115Ala
XM_017027544.1:c.6344A>C	XP_016883033.1:p.Asp2115Ala
XM_017027545.1:c.5780A>C	XP_016883034.1:p.Asp1927Ala
XM_017027546.1:c.3308A>C	XP_016883035.1:p.Asp1103Ala
NM_014727.3:c.6344A>C MANE Select	NP_055542.1:p.Asp2115Ala