Canonical Allele Identifier: CA475204205

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703706T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936238T>A , CM000673.2:g.68936238T>A	GRCh38
NC_000011.9:g.68703706T>A , CM000673.1:g.68703706T>A	GRCh37
NC_000011.8:g.68460282T>A	NCBI36
NG_007976.1:g.37388T>A , LRG_250:g.37388T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1758T>A MANE Select	ENSP00000255078.4:p.Gly586=
ENST00000674675.1:c.2T>A
ENST00000674878.1:c.2T>A
ENST00000674955.1:c.*475T>A	ENSP00000502463.1:n.*475T>A
ENST00000675118.1:c.1246T>A
ENST00000675389.1:n.33T>A
ENST00000675615.1:c.1758T>A	ENSP00000502413.1:p.Gly586=
ENST00000675648.1:n.1133T>A
ENST00000675916.1:c.2T>A
ENST00000676173.1:n.2503T>A
ENST00000676182.1:c.189T>A
ENST00000676228.1:c.*1081T>A	ENSP00000502375.1:n.*1081T>A
ENST00000255078.7:c.1758T>A	ENSP00000255078.3:p.Gly586=
ENST00000539064.5:n.1517T>A
ENST00000541229.5:n.453T>A
ENST00000543739.5:n.751T>A
ENST00000545475.1:n.354T>A
NM_002180.2:c.1758T>A , LRG_250t1:c.1758T>A	NP_002171.2:p.Gly586=
XM_005273974.2:c.747T>A	XP_005274031.1:p.Gly249=
XM_005273975.2:c.630T>A	XP_005274032.1:p.Gly210=
XM_011544994.1:c.525T>A	XP_011543296.1:p.Gly175=
XR_949903.1:n.1860T>A
XM_005273975.3:c.630T>A	XP_005274032.1:p.Gly210=
XM_017017669.2:c.747T>A	XP_016873158.1:p.Gly249=
XM_017017670.2:c.747T>A	XP_016873159.1:p.Gly249=
XR_949903.3:n.1856T>A
NM_002180.3:c.1758T>A MANE Select	NP_002171.2:p.Gly586=