Canonical Allele Identifier: CA1630848750

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936560C= , CM000673.2:g.68936560C=	GRCh38
NC_000011.9:g.68704028C= , CM000673.1:g.68704028C=	GRCh37
NC_000011.8:g.68460604C=	NCBI36
NG_007976.1:g.37710C= , LRG_250:g.37710C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2080C= MANE Select	ENSP00000255078.4:p.Arg694=
ENST00000674675.1:c.324C=
ENST00000674878.1:c.324C=
ENST00000674955.1:c.*797C=	ENSP00000502463.1:n.*797C=
ENST00000675118.1:c.1568C=
ENST00000675389.1:n.355C=
ENST00000675615.1:c.2080C=	ENSP00000502413.1:p.Arg694=
ENST00000675648.1:n.1455C=
ENST00000675916.1:c.324C=
ENST00000676173.1:n.2825C=
ENST00000676182.1:c.511C=
ENST00000676228.1:c.*1403C=	ENSP00000502375.1:n.*1403C=
ENST00000255078.7:c.2080C=	ENSP00000255078.3:p.Arg694=
ENST00000539064.5:n.1839C=
ENST00000543739.5:n.1073C=
NM_002180.2:c.2080C= , LRG_250t1:c.2080C=	NP_002171.2:p.Arg694=
XM_005273974.2:c.1069C=	XP_005274031.1:p.Arg357=
XM_005273975.2:c.952C=	XP_005274032.1:p.Arg318=
XM_011544994.1:c.847C=	XP_011543296.1:p.Arg283=
XR_949903.1:n.2182C=
XM_005273975.3:c.952C=	XP_005274032.1:p.Arg318=
XM_017017669.2:c.1069C=	XP_016873158.1:p.Arg357=
XM_017017670.2:c.1069C=	XP_016873159.1:p.Arg357=
XR_949903.3:n.2178C=
NM_002180.3:c.2080C= MANE Select	NP_002171.2:p.Arg694=