Canonical Allele Identifier: CA475187123

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68675759A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908291A>C , CM000673.2:g.68908291A>C	GRCh38
NC_000011.9:g.68675759A>C , CM000673.1:g.68675759A>C	GRCh37
NC_000011.8:g.68432335A>C	NCBI36
NG_007976.1:g.9441A>C , LRG_250:g.9441A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.403A>C MANE Select	ENSP00000255078.4:p.Arg135=
ENST00000539224.2:c.366A>C
ENST00000674583.1:c.366A>C
ENST00000674597.1:c.214A>C
ENST00000674955.1:c.403A>C	ENSP00000502463.1:p.Arg135=
ENST00000675142.1:n.366A>C
ENST00000675469.1:c.279A>C
ENST00000675615.1:c.403A>C	ENSP00000502413.1:p.Arg135=
ENST00000675674.1:n.366A>C
ENST00000675873.1:c.366A>C
ENST00000676173.1:n.447A>C
ENST00000676228.1:c.403A>C	ENSP00000502375.1:p.Arg135=
ENST00000255078.7:c.403A>C	ENSP00000255078.3:p.Arg135=
ENST00000539224.1:c.403A>C	ENSP00000440465.1:p.Arg135=
ENST00000544541.1:c.*143A>C	ENSP00000443343.1:n.*143A>C
NM_002180.2:c.403A>C , LRG_250t1:c.403A>C	NP_002171.2:p.Arg135=
XM_005273974.2:c.-609A>C	XP_005274031.1:n.-609A>C
XM_005273976.1:c.403A>C	XP_005274033.1:p.Arg135=
XR_247198.1:n.505A>C
XR_949903.1:n.505A>C
XM_005273976.2:c.403A>C	XP_005274033.1:p.Arg135=
XM_017017669.2:c.-511A>C	XP_016873158.1:n.-511A>C
XM_017017671.2:c.403A>C	XP_016873160.1:p.Arg135=
XR_949903.3:n.501A>C
NM_002180.3:c.403A>C MANE Select	NP_002171.2:p.Arg135=