Canonical Allele Identifier: CA475204292

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703757T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936289T>A , CM000673.2:g.68936289T>A	GRCh38
NC_000011.9:g.68703757T>A , CM000673.1:g.68703757T>A	GRCh37
NC_000011.8:g.68460333T>A	NCBI36
NG_007976.1:g.37439T>A , LRG_250:g.37439T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1809T>A MANE Select	ENSP00000255078.4:p.Arg603=
ENST00000674675.1:c.53T>A
ENST00000674878.1:c.53T>A
ENST00000674955.1:c.*526T>A	ENSP00000502463.1:n.*526T>A
ENST00000675118.1:c.1297T>A
ENST00000675389.1:n.84T>A
ENST00000675615.1:c.1809T>A	ENSP00000502413.1:p.Arg603=
ENST00000675648.1:n.1184T>A
ENST00000675916.1:c.53T>A
ENST00000676173.1:n.2554T>A
ENST00000676182.1:c.240T>A
ENST00000676228.1:c.*1132T>A	ENSP00000502375.1:n.*1132T>A
ENST00000255078.7:c.1809T>A	ENSP00000255078.3:p.Arg603=
ENST00000539064.5:n.1568T>A
ENST00000541229.5:n.504T>A
ENST00000543739.5:n.802T>A
ENST00000545475.1:n.405T>A
NM_002180.2:c.1809T>A , LRG_250t1:c.1809T>A	NP_002171.2:p.Arg603=
XM_005273974.2:c.798T>A	XP_005274031.1:p.Arg266=
XM_005273975.2:c.681T>A	XP_005274032.1:p.Arg227=
XM_011544994.1:c.576T>A	XP_011543296.1:p.Arg192=
XR_949903.1:n.1911T>A
XM_005273975.3:c.681T>A	XP_005274032.1:p.Arg227=
XM_017017669.2:c.798T>A	XP_016873158.1:p.Arg266=
XM_017017670.2:c.798T>A	XP_016873159.1:p.Arg266=
XR_949903.3:n.1907T>A
NM_002180.3:c.1809T>A MANE Select	NP_002171.2:p.Arg603=