Canonical Allele Identifier: CA381652964

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704122G>A (hg19) ; chr11:g.68936654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936654G>A , CM000673.2:g.68936654G>A	GRCh38
NC_000011.9:g.68704122G>A , CM000673.1:g.68704122G>A	GRCh37
NC_000011.8:g.68460698G>A	NCBI36
NG_007976.1:g.37804G>A , LRG_250:g.37804G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2174G>A MANE Select	ENSP00000255078.4:p.Gly725Asp
ENST00000674675.1:c.418G>A
ENST00000674878.1:c.418G>A
ENST00000674955.1:c.*891G>A	ENSP00000502463.1:n.*891G>A
ENST00000675118.1:c.1662G>A
ENST00000675389.1:n.449G>A
ENST00000675615.1:c.2174G>A	ENSP00000502413.1:p.Gly725Asp
ENST00000675648.1:n.1549G>A
ENST00000675916.1:c.418G>A
ENST00000676173.1:n.2919G>A
ENST00000676182.1:c.605G>A
ENST00000676228.1:c.*1497G>A	ENSP00000502375.1:n.*1497G>A
ENST00000255078.7:c.2174G>A	ENSP00000255078.3:p.Gly725Asp
ENST00000539064.5:n.1933G>A
ENST00000543739.5:n.1167G>A
NM_002180.2:c.2174G>A , LRG_250t1:c.2174G>A	NP_002171.2:p.Gly725Asp
XM_005273974.2:c.1163G>A	XP_005274031.1:p.Gly388Asp
XM_005273975.2:c.1046G>A	XP_005274032.1:p.Gly349Asp
XM_011544994.1:c.941G>A	XP_011543296.1:p.Gly314Asp
XR_949903.1:n.2276G>A
XM_005273975.3:c.1046G>A	XP_005274032.1:p.Gly349Asp
XM_017017669.2:c.1163G>A	XP_016873158.1:p.Gly388Asp
XM_017017670.2:c.1163G>A	XP_016873159.1:p.Gly388Asp
XR_949903.3:n.2272G>A
NM_002180.3:c.2174G>A MANE Select	NP_002171.2:p.Gly725Asp