Canonical Allele Identifier: CA405418750

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220893G>C (hg19) ; chr19:g.35729992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35729992G>C , CM000681.2:g.35729992G>C	GRCh38
NC_000019.9:g.36220893G>C , CM000681.1:g.36220893G>C	GRCh37
NC_000019.8:g.40912733G>C	NCBI36
NG_052906.1:g.16974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4877G>C	ENSP00000501283.1:p.Gly1626Ala
ENST00000674114.2:c.2484G>C	ENSP00000501039.2:n.2484G>C
ENST00000684977.1:c.161G>C	ENSP00000509384.1:p.Gly54Ala
ENST00000685168.1:c.369G>C
ENST00000689544.1:n.96G>C
ENST00000691421.1:c.164G>C	ENSP00000508674.1:p.Gly55Ala
ENST00000691855.1:c.4485G>C
ENST00000692961.1:c.4943G>C	ENSP00000509289.1:p.Gly1648Ala
ENST00000420124.4:c.4943G>C MANE Select	ENSP00000398837.2:p.Gly1648Ala
ENST00000673918.1:c.4877G>C	ENSP00000501283.1:p.Gly1626Ala
ENST00000674114.1:c.2265G>C
ENST00000420124.2:c.4943G>C	ENSP00000398837.1:p.Gly1648Ala
NM_014727.2:c.4943G>C	NP_055542.1:p.Gly1648Ala
XM_011527561.1:c.4877G>C	XP_011525863.1:p.Gly1626Ala
XM_011527562.1:c.4943G>C	XP_011525864.1:p.Gly1648Ala
XM_011527563.1:c.4667G>C	XP_011525865.1:p.Gly1556Ala
XM_011527561.2:c.4379G>C	XP_011525863.2:p.Gly1460Ala
XM_011527562.2:c.4943G>C	XP_011525864.1:p.Gly1648Ala
XM_017027544.1:c.4943G>C	XP_016883033.1:p.Gly1648Ala
XM_017027545.1:c.4379G>C	XP_016883034.1:p.Gly1460Ala
XM_017027546.1:c.1907G>C	XP_016883035.1:p.Gly636Ala
NM_014727.3:c.4943G>C MANE Select	NP_055542.1:p.Gly1648Ala