Canonical Allele Identifier: CA381653701

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704407G>A (hg19) ; chr11:g.68936939G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936939G>A , CM000673.2:g.68936939G>A	GRCh38
NC_000011.9:g.68704407G>A , CM000673.1:g.68704407G>A	GRCh37
NC_000011.8:g.68460983G>A	NCBI36
NG_007976.1:g.38089G>A , LRG_250:g.38089G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2459G>A MANE Select	ENSP00000255078.4:p.Arg820Lys
ENST00000674675.1:c.604G>A
ENST00000674878.1:c.564G>A
ENST00000675118.1:c.1947G>A
ENST00000675389.1:n.734G>A
ENST00000675615.1:c.2459G>A	ENSP00000502413.1:p.Arg820Lys
ENST00000675648.1:n.1834G>A
ENST00000675916.1:c.703G>A
ENST00000676173.1:n.3204G>A
ENST00000676182.1:c.890G>A
ENST00000676228.1:c.*1782G>A	ENSP00000502375.1:n.*1782G>A
ENST00000255078.7:c.2459G>A	ENSP00000255078.3:p.Arg820Lys
ENST00000539064.5:n.2218G>A
ENST00000543739.5:n.1452G>A
NM_002180.2:c.2459G>A , LRG_250t1:c.2459G>A	NP_002171.2:p.Arg820Lys
XM_005273974.2:c.1448G>A	XP_005274031.1:p.Arg483Lys
XM_005273975.2:c.1331G>A	XP_005274032.1:p.Arg444Lys
XM_011544994.1:c.1226G>A	XP_011543296.1:p.Arg409Lys
XR_949903.1:n.2561G>A
XM_005273975.3:c.1331G>A	XP_005274032.1:p.Arg444Lys
XM_017017669.2:c.1448G>A	XP_016873158.1:p.Arg483Lys
XM_017017670.2:c.1448G>A	XP_016873159.1:p.Arg483Lys
XR_949903.3:n.2557G>A
NM_002180.3:c.2459G>A MANE Select	NP_002171.2:p.Arg820Lys