Canonical Allele Identifier: CA405419309

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36221001A>C (hg19) ; chr19:g.35730100A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35730100A>C , CM000681.2:g.35730100A>C	GRCh38
NC_000019.9:g.36221001A>C , CM000681.1:g.36221001A>C	GRCh37
NC_000019.8:g.40912841A>C	NCBI36
NG_052906.1:g.17082A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673918.2:c.4985A>C	ENSP00000501283.1:p.Lys1662Thr
ENST00000674114.2:c.2592A>C	ENSP00000501039.2:n.2592A>C
ENST00000684977.1:c.269A>C	ENSP00000509384.1:p.Lys90Thr
ENST00000685168.1:c.477A>C
ENST00000689544.1:n.204A>C
ENST00000691421.1:c.272A>C	ENSP00000508674.1:p.Lys91Thr
ENST00000691855.1:c.4593A>C
ENST00000692961.1:c.5051A>C	ENSP00000509289.1:p.Lys1684Thr
ENST00000420124.4:c.5051A>C MANE Select	ENSP00000398837.2:p.Lys1684Thr
ENST00000673918.1:c.4985A>C	ENSP00000501283.1:p.Lys1662Thr
ENST00000674114.1:c.2373A>C
ENST00000420124.2:c.5051A>C	ENSP00000398837.1:p.Lys1684Thr
NM_014727.2:c.5051A>C	NP_055542.1:p.Lys1684Thr
XM_011527561.1:c.4985A>C	XP_011525863.1:p.Lys1662Thr
XM_011527562.1:c.5051A>C	XP_011525864.1:p.Lys1684Thr
XM_011527563.1:c.4775A>C	XP_011525865.1:p.Lys1592Thr
XM_011527561.2:c.4487A>C	XP_011525863.2:p.Lys1496Thr
XM_011527562.2:c.5051A>C	XP_011525864.1:p.Lys1684Thr
XM_017027544.1:c.5051A>C	XP_016883033.1:p.Lys1684Thr
XM_017027545.1:c.4487A>C	XP_016883034.1:p.Lys1496Thr
XM_017027546.1:c.2015A>C	XP_016883035.1:p.Lys672Thr
NM_014727.3:c.5051A>C MANE Select	NP_055542.1:p.Lys1684Thr