Canonical Allele Identifier: CA2581029157

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936491A= , CM000673.2:g.68936491A=	GRCh38
NC_000011.9:g.68703959A= , CM000673.1:g.68703959A=	GRCh37
NC_000011.8:g.68460535A=	NCBI36
NG_007976.1:g.37641A= , LRG_250:g.37641A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2011A= MANE Select	ENSP00000255078.4:p.Thr671=
ENST00000674675.1:c.255A=
ENST00000674878.1:c.255A=
ENST00000674955.1:c.*728A=	ENSP00000502463.1:n.*728A=
ENST00000675118.1:c.1499A=
ENST00000675389.1:n.286A=
ENST00000675615.1:c.2011A=	ENSP00000502413.1:p.Thr671=
ENST00000675648.1:n.1386A=
ENST00000675916.1:c.255A=
ENST00000676173.1:n.2756A=
ENST00000676182.1:c.442A=
ENST00000676228.1:c.*1334A=	ENSP00000502375.1:n.*1334A=
ENST00000255078.7:c.2011A=	ENSP00000255078.3:p.Thr671=
ENST00000539064.5:n.1770A=
ENST00000543739.5:n.1004A=
NM_002180.2:c.2011A= , LRG_250t1:c.2011A=	NP_002171.2:p.Thr671=
XM_005273974.2:c.1000A=	XP_005274031.1:p.Thr334=
XM_005273975.2:c.883A=	XP_005274032.1:p.Thr295=
XM_011544994.1:c.778A=	XP_011543296.1:p.Thr260=
XR_949903.1:n.2113A=
XM_005273975.3:c.883A=	XP_005274032.1:p.Thr295=
XM_017017669.2:c.1000A=	XP_016873158.1:p.Thr334=
XM_017017670.2:c.1000A=	XP_016873159.1:p.Thr334=
XR_949903.3:n.2109A=
NM_002180.3:c.2011A= MANE Select	NP_002171.2:p.Thr671=