Canonical Allele Identifier: CA381644379

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68682375G>C (hg19) ; chr11:g.68914907G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914907G>C , CM000673.2:g.68914907G>C	GRCh38
NC_000011.9:g.68682375G>C , CM000673.1:g.68682375G>C	GRCh37
NC_000011.8:g.68438951G>C	NCBI36
NG_007976.1:g.16057G>C , LRG_250:g.16057G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.796G>C MANE Select	ENSP00000255078.4:p.Gly266Arg
ENST00000539224.2:c.925G>C
ENST00000674955.1:c.796G>C	ENSP00000502463.1:p.Gly266Arg
ENST00000675118.1:c.143G>C
ENST00000675119.1:c.85G>C	ENSP00000501861.1:p.Gly29Arg
ENST00000675305.1:c.85G>C	ENSP00000502365.1:p.Gly29Arg
ENST00000675464.1:c.85G>C	ENSP00000502650.1:p.Gly29Arg
ENST00000675615.1:c.796G>C	ENSP00000502413.1:p.Gly266Arg
ENST00000675683.1:c.183G>C
ENST00000676173.1:n.840G>C
ENST00000676228.1:c.*119G>C	ENSP00000502375.1:n.*119G>C
ENST00000676239.1:n.110G>C
ENST00000255078.7:c.796G>C	ENSP00000255078.3:p.Gly266Arg
ENST00000539224.1:c.*119G>C	ENSP00000440465.1:n.*119G>C
NM_002180.2:c.796G>C , LRG_250t1:c.796G>C	NP_002171.2:p.Gly266Arg
XM_005273974.2:c.-216G>C	XP_005274031.1:n.-216G>C
XM_005273976.1:c.796G>C	XP_005274033.1:p.Gly266Arg
XR_247198.1:n.898G>C
XR_949903.1:n.898G>C
XM_005273976.2:c.796G>C	XP_005274033.1:p.Gly266Arg
XM_017017669.2:c.-216G>C	XP_016873158.1:n.-216G>C
XM_017017670.2:c.-216G>C	XP_016873159.1:n.-216G>C
XM_017017671.2:c.796G>C	XP_016873160.1:p.Gly266Arg
XR_949903.3:n.894G>C
NM_002180.3:c.796G>C MANE Select	NP_002171.2:p.Gly266Arg