Canonical Allele Identifier: CA405418709

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220883C>G (hg19) ; chr19:g.35729982C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729982C>G , CM000681.2:g.35729982C>G	GRCh38
NC_000019.9:g.36220883C>G , CM000681.1:g.36220883C>G	GRCh37
NC_000019.8:g.40912723C>G	NCBI36
NG_052906.1:g.16964C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4867C>G	ENSP00000501283.1:p.Leu1623Val
ENST00000674114.2:c.2474C>G	ENSP00000501039.2:n.2474C>G
ENST00000684977.1:c.151C>G	ENSP00000509384.1:p.Leu51Val
ENST00000685168.1:c.359C>G
ENST00000689544.1:n.86C>G
ENST00000691421.1:c.154C>G	ENSP00000508674.1:p.Leu52Val
ENST00000691855.1:c.4475C>G
ENST00000692961.1:c.4933C>G	ENSP00000509289.1:p.Leu1645Val
ENST00000420124.4:c.4933C>G MANE Select	ENSP00000398837.2:p.Leu1645Val
ENST00000673918.1:c.4867C>G	ENSP00000501283.1:p.Leu1623Val
ENST00000674114.1:c.2255C>G
ENST00000420124.2:c.4933C>G	ENSP00000398837.1:p.Leu1645Val
NM_014727.2:c.4933C>G	NP_055542.1:p.Leu1645Val
XM_011527561.1:c.4867C>G	XP_011525863.1:p.Leu1623Val
XM_011527562.1:c.4933C>G	XP_011525864.1:p.Leu1645Val
XM_011527563.1:c.4657C>G	XP_011525865.1:p.Leu1553Val
XM_011527561.2:c.4369C>G	XP_011525863.2:p.Leu1457Val
XM_011527562.2:c.4933C>G	XP_011525864.1:p.Leu1645Val
XM_017027544.1:c.4933C>G	XP_016883033.1:p.Leu1645Val
XM_017027545.1:c.4369C>G	XP_016883034.1:p.Leu1457Val
XM_017027546.1:c.1897C>G	XP_016883035.1:p.Leu633Val
NM_014727.3:c.4933C>G MANE Select	NP_055542.1:p.Leu1645Val