Canonical Allele Identifier: CA405424840

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223415G>C (hg19) ; chr19:g.35732514G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732514G>C , CM000681.2:g.35732514G>C	GRCh38
NC_000019.9:g.36223415G>C , CM000681.1:g.36223415G>C	GRCh37
NC_000019.8:g.40915255G>C	NCBI36
NG_052906.1:g.19496G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.271G>C
ENST00000673918.2:c.5899G>C	ENSP00000501283.1:p.Ala1967Pro
ENST00000674114.2:c.3506G>C	ENSP00000501039.2:n.3506G>C
ENST00000684977.1:c.1183G>C	ENSP00000509384.1:p.Ala395Pro
ENST00000689544.1:n.1118G>C
ENST00000691421.1:c.1186G>C	ENSP00000508674.1:p.Ala396Pro
ENST00000691855.1:c.5507G>C
ENST00000692961.1:c.5965G>C	ENSP00000509289.1:p.Ala1989Pro
ENST00000693677.1:c.704+185G>C	ENSP00000509779.1:n.704+185G>C
ENST00000420124.4:c.5965G>C MANE Select	ENSP00000398837.2:p.Ala1989Pro
ENST00000673918.1:c.5899G>C	ENSP00000501283.1:p.Ala1967Pro
ENST00000674114.1:c.3287G>C
ENST00000420124.2:c.5965G>C	ENSP00000398837.1:p.Ala1989Pro
NM_014727.2:c.5965G>C	NP_055542.1:p.Ala1989Pro
XM_011527561.1:c.5899G>C	XP_011525863.1:p.Ala1967Pro
XM_011527562.1:c.5965G>C	XP_011525864.1:p.Ala1989Pro
XM_011527563.1:c.5689G>C	XP_011525865.1:p.Ala1897Pro
XM_011527561.2:c.5401G>C	XP_011525863.2:p.Ala1801Pro
XM_011527562.2:c.5965G>C	XP_011525864.1:p.Ala1989Pro
XM_017027544.1:c.5965G>C	XP_016883033.1:p.Ala1989Pro
XM_017027545.1:c.5401G>C	XP_016883034.1:p.Ala1801Pro
XM_017027546.1:c.2929G>C	XP_016883035.1:p.Ala977Pro
NM_014727.3:c.5965G>C MANE Select	NP_055542.1:p.Ala1989Pro