Canonical Allele Identifier: CA939172711

Gene: IGHMBP2

Linked Data

• gnomAD v3: 11-68908035-C-CTTTTTTTTTTTTTT
• gnomAD v4: 11-68908035-C-CTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908036_68908037insTTTTTTTTTTTTTT , CM000673.2:g.68908036_68908037insTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68675504_68675505insTTTTTTTTTTTTTT , CM000673.1:g.68675504_68675505insTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68432080_68432081insTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.9186_9187insTTTTTTTTTTTTTT , LRG_250:g.9186_9187insTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-109_257-108insTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.257-109_257-108insTTTTTTTTTTTTTT
ENST00000539224.2:c.220-109_220-108insTTTTTTTTTTTTTT
ENST00000674583.1:c.220-109_220-108insTTTTTTTTTTTTTT
ENST00000674597.1:c.68-109_68-108insTTTTTTTTTTTTTT
ENST00000674955.1:c.257-109_257-108insTTTTTTTTTTTTTT	ENSP00000502463.1:n.257-109_257-108insTTTTTTTTTTTTTT
ENST00000675142.1:n.220-109_220-108insTTTTTTTTTTTTTT
ENST00000675469.1:c.133-109_133-108insTTTTTTTTTTTTTT
ENST00000675615.1:c.257-109_257-108insTTTTTTTTTTTTTT	ENSP00000502413.1:n.257-109_257-108insTTTTTTTTTTTTTT
ENST00000675674.1:n.220-109_220-108insTTTTTTTTTTTTTT
ENST00000675873.1:c.220-109_220-108insTTTTTTTTTTTTTT
ENST00000676173.1:n.301-109_301-108insTTTTTTTTTTTTTT
ENST00000676228.1:c.257-109_257-108insTTTTTTTTTTTTTT	ENSP00000502375.1:n.257-109_257-108insTTTTTTTTTTTTTT
ENST00000255078.7:c.257-109_257-108insTTTTTTTTTTTTTT	ENSP00000255078.3:n.257-109_257-108insTTTTTTTTTTTTTT
ENST00000539224.1:c.257-109_257-108insTTTTTTTTTTTTTT	ENSP00000440465.1:n.257-109_257-108insTTTTTTTTTTTTTT
ENST00000544541.1:c.87-109_87-108insTTTTTTTTTTTTTT	ENSP00000443343.1:n.87-109_87-108insTTTTTTTTTTTTTT
ENST00000545146.1:c.*127-109_*127-108insTTTTTTTTTTTTTT	ENSP00000456366.1:n.*127-109_*127-108insTTTTTTTTTTTTTT
NM_002180.2:c.257-109_257-108insTTTTTTTTTTTTTT , LRG_250t1:c.257-109_257-108insTTTTTTTTTTTTTT	NP_002171.2:n.257-109_257-108insTTTTTTTTTTTTTT
XM_005273974.2:c.-755-109_-755-108insTTTTTTTTTTTTTT	XP_005274031.1:n.-755-109_-755-108insTTTTTTTTTTTTTT
XM_005273976.1:c.257-109_257-108insTTTTTTTTTTTTTT	XP_005274033.1:n.257-109_257-108insTTTTTTTTTTTTTT
XR_247198.1:n.359-109_359-108insTTTTTTTTTTTTTT
XR_949903.1:n.359-109_359-108insTTTTTTTTTTTTTT
XM_005273976.2:c.257-109_257-108insTTTTTTTTTTTTTT	XP_005274033.1:n.257-109_257-108insTTTTTTTTTTTTTT
XM_017017669.2:c.-657-109_-657-108insTTTTTTTTTTTTTT	XP_016873158.1:n.-657-109_-657-108insTTTTTTTTTTTTTT
XM_017017671.2:c.257-109_257-108insTTTTTTTTTTTTTT	XP_016873160.1:n.257-109_257-108insTTTTTTTTTTTTTT
XR_949903.3:n.355-109_355-108insTTTTTTTTTTTTTT
NM_002180.3:c.257-109_257-108insTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.257-109_257-108insTTTTTTTTTTTTTT