Canonical Allele Identifier: CA405431449

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36224662A>C (hg19) ; chr19:g.35733761A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35733761A>C , CM000681.2:g.35733761A>C	GRCh38
NC_000019.9:g.36224662A>C , CM000681.1:g.36224662A>C	GRCh37
NC_000019.8:g.40916502A>C	NCBI36
NG_052906.1:g.20743A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000592092.2:n.1518A>C
ENST00000673918.2:c.6984-2A>C	ENSP00000501283.1:n.6984-2A>C
ENST00000674114.2:c.4591-2A>C	ENSP00000501039.2:n.4591-2A>C
ENST00000684977.1:c.2245-2A>C	ENSP00000509384.1:n.2245-2A>C
ENST00000689544.1:n.2291-2A>C
ENST00000691421.1:c.2181-2A>C	ENSP00000508674.1:n.2181-2A>C
ENST00000691855.1:c.6592-2A>C
ENST00000692961.1:c.6972A>C	ENSP00000509289.1:p.Ala2324=
ENST00000693677.1:c.795-2A>C	ENSP00000509779.1:n.795-2A>C
ENST00000420124.4:c.7050-2A>C MANE Select	ENSP00000398837.2:n.7050-2A>C
ENST00000673918.1:c.6984-2A>C	ENSP00000501283.1:n.6984-2A>C
ENST00000674114.1:c.4372-2A>C
ENST00000420124.2:c.7050-2A>C	ENSP00000398837.1:n.7050-2A>C
ENST00000592092.1:n.430-2A>C
NM_014727.2:c.7050-2A>C	NP_055542.1:n.7050-2A>C
XM_011527561.1:c.6984-2A>C	XP_011525863.1:n.6984-2A>C
XM_011527562.1:c.7050-2A>C	XP_011525864.1:n.7050-2A>C
XM_011527563.1:c.6774-2A>C	XP_011525865.1:n.6774-2A>C
XM_011527561.2:c.6486-2A>C	XP_011525863.2:n.6486-2A>C
XM_011527562.2:c.7050-2A>C	XP_011525864.1:n.7050-2A>C
XM_017027544.1:c.6960-2A>C	XP_016883033.1:n.6960-2A>C
XM_017027545.1:c.6486-2A>C	XP_016883034.1:n.6486-2A>C
XM_017027546.1:c.4014-2A>C	XP_016883035.1:n.4014-2A>C
NM_014727.3:c.7050-2A>C MANE Select	NP_055542.1:n.7050-2A>C