Canonical Allele Identifier: CA405418851

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220913C>G (hg19) ; chr19:g.35730012C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730012C>G , CM000681.2:g.35730012C>G	GRCh38
NC_000019.9:g.36220913C>G , CM000681.1:g.36220913C>G	GRCh37
NC_000019.8:g.40912753C>G	NCBI36
NG_052906.1:g.16994C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4897C>G	ENSP00000501283.1:p.Leu1633Val
ENST00000674114.2:c.2504C>G	ENSP00000501039.2:n.2504C>G
ENST00000684977.1:c.181C>G	ENSP00000509384.1:p.Leu61Val
ENST00000685168.1:c.389C>G
ENST00000689544.1:n.116C>G
ENST00000691421.1:c.184C>G	ENSP00000508674.1:p.Leu62Val
ENST00000691855.1:c.4505C>G
ENST00000692961.1:c.4963C>G	ENSP00000509289.1:p.Leu1655Val
ENST00000420124.4:c.4963C>G MANE Select	ENSP00000398837.2:p.Leu1655Val
ENST00000673918.1:c.4897C>G	ENSP00000501283.1:p.Leu1633Val
ENST00000674114.1:c.2285C>G
ENST00000420124.2:c.4963C>G	ENSP00000398837.1:p.Leu1655Val
NM_014727.2:c.4963C>G	NP_055542.1:p.Leu1655Val
XM_011527561.1:c.4897C>G	XP_011525863.1:p.Leu1633Val
XM_011527562.1:c.4963C>G	XP_011525864.1:p.Leu1655Val
XM_011527563.1:c.4687C>G	XP_011525865.1:p.Leu1563Val
XM_011527561.2:c.4399C>G	XP_011525863.2:p.Leu1467Val
XM_011527562.2:c.4963C>G	XP_011525864.1:p.Leu1655Val
XM_017027544.1:c.4963C>G	XP_016883033.1:p.Leu1655Val
XM_017027545.1:c.4399C>G	XP_016883034.1:p.Leu1467Val
XM_017027546.1:c.1927C>G	XP_016883035.1:p.Leu643Val
NM_014727.3:c.4963C>G MANE Select	NP_055542.1:p.Leu1655Val