Canonical Allele Identifier: CA381653161

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704209A>T (hg19) ; chr11:g.68936741A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936741A>T , CM000673.2:g.68936741A>T	GRCh38
NC_000011.9:g.68704209A>T , CM000673.1:g.68704209A>T	GRCh37
NC_000011.8:g.68460785A>T	NCBI36
NG_007976.1:g.37891A>T , LRG_250:g.37891A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2261A>T MANE Select	ENSP00000255078.4:p.Asp754Val
ENST00000674675.1:c.505A>T
ENST00000674878.1:c.505A>T
ENST00000674955.1:c.*978A>T	ENSP00000502463.1:n.*978A>T
ENST00000675118.1:c.1749A>T
ENST00000675389.1:n.536A>T
ENST00000675615.1:c.2261A>T	ENSP00000502413.1:p.Asp754Val
ENST00000675648.1:n.1636A>T
ENST00000675916.1:c.505A>T
ENST00000676173.1:n.3006A>T
ENST00000676182.1:c.692A>T
ENST00000676228.1:c.*1584A>T	ENSP00000502375.1:n.*1584A>T
ENST00000255078.7:c.2261A>T	ENSP00000255078.3:p.Asp754Val
ENST00000539064.5:n.2020A>T
ENST00000543739.5:n.1254A>T
NM_002180.2:c.2261A>T , LRG_250t1:c.2261A>T	NP_002171.2:p.Asp754Val
XM_005273974.2:c.1250A>T	XP_005274031.1:p.Asp417Val
XM_005273975.2:c.1133A>T	XP_005274032.1:p.Asp378Val
XM_011544994.1:c.1028A>T	XP_011543296.1:p.Asp343Val
XR_949903.1:n.2363A>T
XM_005273975.3:c.1133A>T	XP_005274032.1:p.Asp378Val
XM_017017669.2:c.1250A>T	XP_016873158.1:p.Asp417Val
XM_017017670.2:c.1250A>T	XP_016873159.1:p.Asp417Val
XR_949903.3:n.2359A>T
NM_002180.3:c.2261A>T MANE Select	NP_002171.2:p.Asp754Val