Canonical Allele Identifier: CA475204212

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703712T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936244T>A , CM000673.2:g.68936244T>A	GRCh38
NC_000011.9:g.68703712T>A , CM000673.1:g.68703712T>A	GRCh37
NC_000011.8:g.68460288T>A	NCBI36
NG_007976.1:g.37394T>A , LRG_250:g.37394T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1764T>A MANE Select	ENSP00000255078.4:p.Val588=
ENST00000674675.1:c.8T>A
ENST00000674878.1:c.8T>A
ENST00000674955.1:c.*481T>A	ENSP00000502463.1:n.*481T>A
ENST00000675118.1:c.1252T>A
ENST00000675389.1:n.39T>A
ENST00000675615.1:c.1764T>A	ENSP00000502413.1:p.Val588=
ENST00000675648.1:n.1139T>A
ENST00000675916.1:c.8T>A
ENST00000676173.1:n.2509T>A
ENST00000676182.1:c.195T>A
ENST00000676228.1:c.*1087T>A	ENSP00000502375.1:n.*1087T>A
ENST00000255078.7:c.1764T>A	ENSP00000255078.3:p.Val588=
ENST00000539064.5:n.1523T>A
ENST00000541229.5:n.459T>A
ENST00000543739.5:n.757T>A
ENST00000545475.1:n.360T>A
NM_002180.2:c.1764T>A , LRG_250t1:c.1764T>A	NP_002171.2:p.Val588=
XM_005273974.2:c.753T>A	XP_005274031.1:p.Val251=
XM_005273975.2:c.636T>A	XP_005274032.1:p.Val212=
XM_011544994.1:c.531T>A	XP_011543296.1:p.Val177=
XR_949903.1:n.1866T>A
XM_005273975.3:c.636T>A	XP_005274032.1:p.Val212=
XM_017017669.2:c.753T>A	XP_016873158.1:p.Val251=
XM_017017670.2:c.753T>A	XP_016873159.1:p.Val251=
XR_949903.3:n.1862T>A
NM_002180.3:c.1764T>A MANE Select	NP_002171.2:p.Val588=