Canonical Allele Identifier: CA475280703

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704150G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936682G>A , CM000673.2:g.68936682G>A	GRCh38
NC_000011.9:g.68704150G>A , CM000673.1:g.68704150G>A	GRCh37
NC_000011.8:g.68460726G>A	NCBI36
NG_007976.1:g.37832G>A , LRG_250:g.37832G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2202G>A MANE Select	ENSP00000255078.4:p.Val734=
ENST00000674675.1:c.446G>A
ENST00000674878.1:c.446G>A
ENST00000674955.1:c.*919G>A	ENSP00000502463.1:n.*919G>A
ENST00000675118.1:c.1690G>A
ENST00000675389.1:n.477G>A
ENST00000675615.1:c.2202G>A	ENSP00000502413.1:p.Val734=
ENST00000675648.1:n.1577G>A
ENST00000675916.1:c.446G>A
ENST00000676173.1:n.2947G>A
ENST00000676182.1:c.633G>A
ENST00000676228.1:c.*1525G>A	ENSP00000502375.1:n.*1525G>A
ENST00000255078.7:c.2202G>A	ENSP00000255078.3:p.Val734=
ENST00000539064.5:n.1961G>A
ENST00000543739.5:n.1195G>A
NM_002180.2:c.2202G>A , LRG_250t1:c.2202G>A	NP_002171.2:p.Val734=
XM_005273974.2:c.1191G>A	XP_005274031.1:p.Val397=
XM_005273975.2:c.1074G>A	XP_005274032.1:p.Val358=
XM_011544994.1:c.969G>A	XP_011543296.1:p.Val323=
XR_949903.1:n.2304G>A
XM_005273975.3:c.1074G>A	XP_005274032.1:p.Val358=
XM_017017669.2:c.1191G>A	XP_016873158.1:p.Val397=
XM_017017670.2:c.1191G>A	XP_016873159.1:p.Val397=
XR_949903.3:n.2300G>A
NM_002180.3:c.2202G>A MANE Select	NP_002171.2:p.Val734=