Canonical Allele Identifier: CA381651581

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703755C>A (hg19) ; chr11:g.68936287C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936287C>A , CM000673.2:g.68936287C>A	GRCh38
NC_000011.9:g.68703755C>A , CM000673.1:g.68703755C>A	GRCh37
NC_000011.8:g.68460331C>A	NCBI36
NG_007976.1:g.37437C>A , LRG_250:g.37437C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1807C>A MANE Select	ENSP00000255078.4:p.Arg603Ser
ENST00000674675.1:c.51C>A
ENST00000674878.1:c.51C>A
ENST00000674955.1:c.*524C>A	ENSP00000502463.1:n.*524C>A
ENST00000675118.1:c.1295C>A
ENST00000675389.1:n.82C>A
ENST00000675615.1:c.1807C>A	ENSP00000502413.1:p.Arg603Ser
ENST00000675648.1:n.1182C>A
ENST00000675916.1:c.51C>A
ENST00000676173.1:n.2552C>A
ENST00000676182.1:c.238C>A
ENST00000676228.1:c.*1130C>A	ENSP00000502375.1:n.*1130C>A
ENST00000255078.7:c.1807C>A	ENSP00000255078.3:p.Arg603Ser
ENST00000539064.5:n.1566C>A
ENST00000541229.5:n.502C>A
ENST00000543739.5:n.800C>A
ENST00000545475.1:n.403C>A
NM_002180.2:c.1807C>A , LRG_250t1:c.1807C>A	NP_002171.2:p.Arg603Ser
XM_005273974.2:c.796C>A	XP_005274031.1:p.Arg266Ser
XM_005273975.2:c.679C>A	XP_005274032.1:p.Arg227Ser
XM_011544994.1:c.574C>A	XP_011543296.1:p.Arg192Ser
XR_949903.1:n.1909C>A
XM_005273975.3:c.679C>A	XP_005274032.1:p.Arg227Ser
XM_017017669.2:c.796C>A	XP_016873158.1:p.Arg266Ser
XM_017017670.2:c.796C>A	XP_016873159.1:p.Arg266Ser
XR_949903.3:n.1905C>A
NM_002180.3:c.1807C>A MANE Select	NP_002171.2:p.Arg603Ser