Canonical Allele Identifier: CA507308622

Gene: KMT2B

Linked Data

• gnomAD v4: 19-35732894-T-C
• MyVariant Identifiers: chr19:g.36223795T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732894T>C , CM000681.2:g.35732894T>C	GRCh38
NC_000019.9:g.36223795T>C , CM000681.1:g.36223795T>C	GRCh37
NC_000019.8:g.40915635T>C	NCBI36
NG_052906.1:g.19876T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.651T>C
ENST00000673918.2:c.6279T>C	ENSP00000501283.1:p.Asp2093=
ENST00000674114.2:c.3886T>C	ENSP00000501039.2:n.3886T>C
ENST00000684977.1:c.1563T>C	ENSP00000509384.1:p.Asp521=
ENST00000689544.1:n.1498T>C
ENST00000691421.1:c.1566T>C	ENSP00000508674.1:p.Asp522=
ENST00000691855.1:c.5887T>C
ENST00000692961.1:c.6345T>C	ENSP00000509289.1:p.Asp2115=
ENST00000693677.1:c.704+565T>C	ENSP00000509779.1:n.704+565T>C
ENST00000420124.4:c.6345T>C MANE Select	ENSP00000398837.2:p.Asp2115=
ENST00000673918.1:c.6279T>C	ENSP00000501283.1:p.Asp2093=
ENST00000674114.1:c.3667T>C
ENST00000420124.2:c.6345T>C	ENSP00000398837.1:p.Asp2115=
NM_014727.2:c.6345T>C	NP_055542.1:p.Asp2115=
XM_011527561.1:c.6279T>C	XP_011525863.1:p.Asp2093=
XM_011527562.1:c.6345T>C	XP_011525864.1:p.Asp2115=
XM_011527563.1:c.6069T>C	XP_011525865.1:p.Asp2023=
XM_011527561.2:c.5781T>C	XP_011525863.2:p.Asp1927=
XM_011527562.2:c.6345T>C	XP_011525864.1:p.Asp2115=
XM_017027544.1:c.6345T>C	XP_016883033.1:p.Asp2115=
XM_017027545.1:c.5781T>C	XP_016883034.1:p.Asp1927=
XM_017027546.1:c.3309T>C	XP_016883035.1:p.Asp1103=
NM_014727.3:c.6345T>C MANE Select	NP_055542.1:p.Asp2115=