Canonical Allele Identifier: CA9385636

Gene: KMT2B

Linked Data

• ClinVar Variation Id: 2184786
• ClinVar RCV Id: RCV002619572
• dbSNP Id: rs368981212
• ExAC: 19:36223671 C / T
• gnomAD v2: 19-36223671-C-T
• gnomAD v3: 19-35732770-C-T
• gnomAD v4: 19-35732770-C-T
• MyVariant Identifiers: chr19:g.36223671C>T (hg19) ; chr19:g.35732770C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732770C>T , CM000681.2:g.35732770C>T	GRCh38
NC_000019.9:g.36223671C>T , CM000681.1:g.36223671C>T	GRCh37
NC_000019.8:g.40915511C>T	NCBI36
NG_052906.1:g.19752C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.527C>T
ENST00000673918.2:c.6155C>T	ENSP00000501283.1:p.Ala2052Val
ENST00000674114.2:c.3762C>T	ENSP00000501039.2:n.3762C>T
ENST00000684977.1:c.1439C>T	ENSP00000509384.1:p.Ala480Val
ENST00000689544.1:n.1374C>T
ENST00000691421.1:c.1442C>T	ENSP00000508674.1:p.Ala481Val
ENST00000691855.1:c.5763C>T
ENST00000692961.1:c.6221C>T	ENSP00000509289.1:p.Ala2074Val
ENST00000693677.1:c.704+441C>T	ENSP00000509779.1:n.704+441C>T
ENST00000420124.4:c.6221C>T MANE Select	ENSP00000398837.2:p.Ala2074Val
ENST00000673918.1:c.6155C>T	ENSP00000501283.1:p.Ala2052Val
ENST00000674114.1:c.3543C>T
ENST00000420124.2:c.6221C>T	ENSP00000398837.1:p.Ala2074Val
NM_014727.2:c.6221C>T	NP_055542.1:p.Ala2074Val
XM_011527561.1:c.6155C>T	XP_011525863.1:p.Ala2052Val
XM_011527562.1:c.6221C>T	XP_011525864.1:p.Ala2074Val
XM_011527563.1:c.5945C>T	XP_011525865.1:p.Ala1982Val
XM_011527561.2:c.5657C>T	XP_011525863.2:p.Ala1886Val
XM_011527562.2:c.6221C>T	XP_011525864.1:p.Ala2074Val
XM_017027544.1:c.6221C>T	XP_016883033.1:p.Ala2074Val
XM_017027545.1:c.5657C>T	XP_016883034.1:p.Ala1886Val
XM_017027546.1:c.3185C>T	XP_016883035.1:p.Ala1062Val
NM_014727.3:c.6221C>T MANE Select	NP_055542.1:p.Ala2074Val