Canonical Allele Identifier: CA2497320958

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1858270679
• gnomAD v4: 11-68908001-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908001_68908002insC , CM000673.2:g.68908001_68908002insC	GRCh38
NC_000011.9:g.68675469_68675470insC , CM000673.1:g.68675469_68675470insC	GRCh37
NC_000011.8:g.68432045_68432046insC	NCBI36
NG_007976.1:g.9151_9152insC , LRG_250:g.9151_9152insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-144_257-143insC MANE Select	ENSP00000255078.4:n.257-144_257-143insC
ENST00000539224.2:c.220-144_220-143insC
ENST00000674583.1:c.220-144_220-143insC
ENST00000674597.1:c.68-144_68-143insC
ENST00000674955.1:c.257-144_257-143insC	ENSP00000502463.1:n.257-144_257-143insC
ENST00000675142.1:n.220-144_220-143insC
ENST00000675469.1:c.133-144_133-143insC
ENST00000675615.1:c.257-144_257-143insC	ENSP00000502413.1:n.257-144_257-143insC
ENST00000675674.1:n.220-144_220-143insC
ENST00000675873.1:c.220-144_220-143insC
ENST00000676173.1:n.301-144_301-143insC
ENST00000676228.1:c.257-144_257-143insC	ENSP00000502375.1:n.257-144_257-143insC
ENST00000255078.7:c.257-144_257-143insC	ENSP00000255078.3:n.257-144_257-143insC
ENST00000539224.1:c.257-144_257-143insC	ENSP00000440465.1:n.257-144_257-143insC
ENST00000544541.1:c.87-144_87-143insC	ENSP00000443343.1:n.87-144_87-143insC
ENST00000545146.1:c.*127-144_*127-143insC	ENSP00000456366.1:n.*127-144_*127-143insC
NM_002180.2:c.257-144_257-143insC , LRG_250t1:c.257-144_257-143insC	NP_002171.2:n.257-144_257-143insC
XM_005273974.2:c.-755-144_-755-143insC	XP_005274031.1:n.-755-144_-755-143insC
XM_005273976.1:c.257-144_257-143insC	XP_005274033.1:n.257-144_257-143insC
XR_247198.1:n.359-144_359-143insC
XR_949903.1:n.359-144_359-143insC
XM_005273976.2:c.257-144_257-143insC	XP_005274033.1:n.257-144_257-143insC
XM_017017669.2:c.-657-144_-657-143insC	XP_016873158.1:n.-657-144_-657-143insC
XM_017017671.2:c.257-144_257-143insC	XP_016873160.1:n.257-144_257-143insC
XR_949903.3:n.355-144_355-143insC
NM_002180.3:c.257-144_257-143insC MANE Select	NP_002171.2:n.257-144_257-143insC