Canonical Allele Identifier: CA679620082

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1174551968
• gnomAD v3: 11-68908003-T-TC
• gnomAD v4: 11-68908003-T-TC
• MyVariant Identifiers: chr11:g.68675471_68675472insC (hg19) ; chr11:g.68908003_68908004insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908003_68908004insC , CM000673.2:g.68908003_68908004insC	GRCh38
NC_000011.9:g.68675471_68675472insC , CM000673.1:g.68675471_68675472insC	GRCh37
NC_000011.8:g.68432047_68432048insC	NCBI36
NG_007976.1:g.9153_9154insC , LRG_250:g.9153_9154insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-142_257-141insC MANE Select	ENSP00000255078.4:n.257-142_257-141insC
ENST00000539224.2:c.220-142_220-141insC
ENST00000674583.1:c.220-142_220-141insC
ENST00000674597.1:c.68-142_68-141insC
ENST00000674955.1:c.257-142_257-141insC	ENSP00000502463.1:n.257-142_257-141insC
ENST00000675142.1:n.220-142_220-141insC
ENST00000675469.1:c.133-142_133-141insC
ENST00000675615.1:c.257-142_257-141insC	ENSP00000502413.1:n.257-142_257-141insC
ENST00000675674.1:n.220-142_220-141insC
ENST00000675873.1:c.220-142_220-141insC
ENST00000676173.1:n.301-142_301-141insC
ENST00000676228.1:c.257-142_257-141insC	ENSP00000502375.1:n.257-142_257-141insC
ENST00000255078.7:c.257-142_257-141insC	ENSP00000255078.3:n.257-142_257-141insC
ENST00000539224.1:c.257-142_257-141insC	ENSP00000440465.1:n.257-142_257-141insC
ENST00000544541.1:c.87-142_87-141insC	ENSP00000443343.1:n.87-142_87-141insC
ENST00000545146.1:c.*127-142_*127-141insC	ENSP00000456366.1:n.*127-142_*127-141insC
NM_002180.2:c.257-142_257-141insC , LRG_250t1:c.257-142_257-141insC	NP_002171.2:n.257-142_257-141insC
XM_005273974.2:c.-755-142_-755-141insC	XP_005274031.1:n.-755-142_-755-141insC
XM_005273976.1:c.257-142_257-141insC	XP_005274033.1:n.257-142_257-141insC
XR_247198.1:n.359-142_359-141insC
XR_949903.1:n.359-142_359-141insC
XM_005273976.2:c.257-142_257-141insC	XP_005274033.1:n.257-142_257-141insC
XM_017017669.2:c.-657-142_-657-141insC	XP_016873158.1:n.-657-142_-657-141insC
XM_017017671.2:c.257-142_257-141insC	XP_016873160.1:n.257-142_257-141insC
XR_949903.3:n.355-142_355-141insC
NM_002180.3:c.257-142_257-141insC MANE Select	NP_002171.2:n.257-142_257-141insC