Canonical Allele Identifier: CA405419067

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36220959G>C (hg19) ; chr19:g.35730058G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730058G>C , CM000681.2:g.35730058G>C	GRCh38
NC_000019.9:g.36220959G>C , CM000681.1:g.36220959G>C	GRCh37
NC_000019.8:g.40912799G>C	NCBI36
NG_052906.1:g.17040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4943G>C	ENSP00000501283.1:p.Ser1648Thr
ENST00000674114.2:c.2550G>C	ENSP00000501039.2:n.2550G>C
ENST00000684977.1:c.227G>C	ENSP00000509384.1:p.Ser76Thr
ENST00000685168.1:c.435G>C
ENST00000689544.1:n.162G>C
ENST00000691421.1:c.230G>C	ENSP00000508674.1:p.Ser77Thr
ENST00000691855.1:c.4551G>C
ENST00000692961.1:c.5009G>C	ENSP00000509289.1:p.Ser1670Thr
ENST00000420124.4:c.5009G>C MANE Select	ENSP00000398837.2:p.Ser1670Thr
ENST00000673918.1:c.4943G>C	ENSP00000501283.1:p.Ser1648Thr
ENST00000674114.1:c.2331G>C
ENST00000420124.2:c.5009G>C	ENSP00000398837.1:p.Ser1670Thr
NM_014727.2:c.5009G>C	NP_055542.1:p.Ser1670Thr
XM_011527561.1:c.4943G>C	XP_011525863.1:p.Ser1648Thr
XM_011527562.1:c.5009G>C	XP_011525864.1:p.Ser1670Thr
XM_011527563.1:c.4733G>C	XP_011525865.1:p.Ser1578Thr
XM_011527561.2:c.4445G>C	XP_011525863.2:p.Ser1482Thr
XM_011527562.2:c.5009G>C	XP_011525864.1:p.Ser1670Thr
XM_017027544.1:c.5009G>C	XP_016883033.1:p.Ser1670Thr
XM_017027545.1:c.4445G>C	XP_016883034.1:p.Ser1482Thr
XM_017027546.1:c.1973G>C	XP_016883035.1:p.Ser658Thr
NM_014727.3:c.5009G>C MANE Select	NP_055542.1:p.Ser1670Thr