Canonical Allele Identifier: CA475280706

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704153G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936685G>A , CM000673.2:g.68936685G>A	GRCh38
NC_000011.9:g.68704153G>A , CM000673.1:g.68704153G>A	GRCh37
NC_000011.8:g.68460729G>A	NCBI36
NG_007976.1:g.37835G>A , LRG_250:g.37835G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2205G>A MANE Select	ENSP00000255078.4:p.Glu735=
ENST00000674675.1:c.449G>A
ENST00000674878.1:c.449G>A
ENST00000674955.1:c.*922G>A	ENSP00000502463.1:n.*922G>A
ENST00000675118.1:c.1693G>A
ENST00000675389.1:n.480G>A
ENST00000675615.1:c.2205G>A	ENSP00000502413.1:p.Glu735=
ENST00000675648.1:n.1580G>A
ENST00000675916.1:c.449G>A
ENST00000676173.1:n.2950G>A
ENST00000676182.1:c.636G>A
ENST00000676228.1:c.*1528G>A	ENSP00000502375.1:n.*1528G>A
ENST00000255078.7:c.2205G>A	ENSP00000255078.3:p.Glu735=
ENST00000539064.5:n.1964G>A
ENST00000543739.5:n.1198G>A
NM_002180.2:c.2205G>A , LRG_250t1:c.2205G>A	NP_002171.2:p.Glu735=
XM_005273974.2:c.1194G>A	XP_005274031.1:p.Glu398=
XM_005273975.2:c.1077G>A	XP_005274032.1:p.Glu359=
XM_011544994.1:c.972G>A	XP_011543296.1:p.Glu324=
XR_949903.1:n.2307G>A
XM_005273975.3:c.1077G>A	XP_005274032.1:p.Glu359=
XM_017017669.2:c.1194G>A	XP_016873158.1:p.Glu398=
XM_017017670.2:c.1194G>A	XP_016873159.1:p.Glu398=
XR_949903.3:n.2303G>A
NM_002180.3:c.2205G>A MANE Select	NP_002171.2:p.Glu735=