Canonical Allele Identifier: CA405428505

Gene: KMT2B

Linked Data

• ClinVar Variation Id: 1184812
• ClinVar RCV Id: RCV001543352
• dbSNP Id: rs2146469485
• MyVariant Identifiers: chr19:g.36223889C>T (hg19) ; chr19:g.35732988C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732988C>T , CM000681.2:g.35732988C>T	GRCh38
NC_000019.9:g.36223889C>T , CM000681.1:g.36223889C>T	GRCh37
NC_000019.8:g.40915729C>T	NCBI36
NG_052906.1:g.19970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.745C>T
ENST00000673918.2:c.6373C>T	ENSP00000501283.1:p.Gln2125Ter
ENST00000674114.2:c.3980C>T	ENSP00000501039.2:n.3980C>T
ENST00000684977.1:c.1657C>T	ENSP00000509384.1:p.Gln553Ter
ENST00000689544.1:n.1592C>T
ENST00000691421.1:c.1660C>T	ENSP00000508674.1:p.Gln554Ter
ENST00000691855.1:c.5981C>T
ENST00000692961.1:c.6439C>T	ENSP00000509289.1:p.Gln2147Ter
ENST00000693677.1:c.705-609C>T	ENSP00000509779.1:n.705-609C>T
ENST00000420124.4:c.6439C>T MANE Select	ENSP00000398837.2:p.Gln2147Ter
ENST00000673918.1:c.6373C>T	ENSP00000501283.1:p.Gln2125Ter
ENST00000674114.1:c.3761C>T
ENST00000420124.2:c.6439C>T	ENSP00000398837.1:p.Gln2147Ter
NM_014727.2:c.6439C>T	NP_055542.1:p.Gln2147Ter
XM_011527561.1:c.6373C>T	XP_011525863.1:p.Gln2125Ter
XM_011527562.1:c.6439C>T	XP_011525864.1:p.Gln2147Ter
XM_011527563.1:c.6163C>T	XP_011525865.1:p.Gln2055Ter
XM_011527561.2:c.5875C>T	XP_011525863.2:p.Gln1959Ter
XM_011527562.2:c.6439C>T	XP_011525864.1:p.Gln2147Ter
XM_017027544.1:c.6439C>T	XP_016883033.1:p.Gln2147Ter
XM_017027545.1:c.5875C>T	XP_016883034.1:p.Gln1959Ter
XM_017027546.1:c.3403C>T	XP_016883035.1:p.Gln1135Ter
NM_014727.3:c.6439C>T MANE Select	NP_055542.1:p.Gln2147Ter