Canonical Allele Identifier: CA405427993

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223804G>C (hg19) ; chr19:g.35732903G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732903G>C , CM000681.2:g.35732903G>C	GRCh38
NC_000019.9:g.36223804G>C , CM000681.1:g.36223804G>C	GRCh37
NC_000019.8:g.40915644G>C	NCBI36
NG_052906.1:g.19885G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.660G>C
ENST00000673918.2:c.6288G>C	ENSP00000501283.1:p.Leu2096Phe
ENST00000674114.2:c.3895G>C	ENSP00000501039.2:n.3895G>C
ENST00000684977.1:c.1572G>C	ENSP00000509384.1:p.Leu524Phe
ENST00000689544.1:n.1507G>C
ENST00000691421.1:c.1575G>C	ENSP00000508674.1:p.Leu525Phe
ENST00000691855.1:c.5896G>C
ENST00000692961.1:c.6354G>C	ENSP00000509289.1:p.Leu2118Phe
ENST00000693677.1:c.704+574G>C	ENSP00000509779.1:n.704+574G>C
ENST00000420124.4:c.6354G>C MANE Select	ENSP00000398837.2:p.Leu2118Phe
ENST00000673918.1:c.6288G>C	ENSP00000501283.1:p.Leu2096Phe
ENST00000674114.1:c.3676G>C
ENST00000420124.2:c.6354G>C	ENSP00000398837.1:p.Leu2118Phe
NM_014727.2:c.6354G>C	NP_055542.1:p.Leu2118Phe
XM_011527561.1:c.6288G>C	XP_011525863.1:p.Leu2096Phe
XM_011527562.1:c.6354G>C	XP_011525864.1:p.Leu2118Phe
XM_011527563.1:c.6078G>C	XP_011525865.1:p.Leu2026Phe
XM_011527561.2:c.5790G>C	XP_011525863.2:p.Leu1930Phe
XM_011527562.2:c.6354G>C	XP_011525864.1:p.Leu2118Phe
XM_017027544.1:c.6354G>C	XP_016883033.1:p.Leu2118Phe
XM_017027545.1:c.5790G>C	XP_016883034.1:p.Leu1930Phe
XM_017027546.1:c.3318G>C	XP_016883035.1:p.Leu1106Phe
NM_014727.3:c.6354G>C MANE Select	NP_055542.1:p.Leu2118Phe