Canonical Allele Identifier: CA939178351

Gene: IGHMBP2

Linked Data

• gnomAD v3: 11-68915166-C-CTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTT
• gnomAD v4: 11-68915166-C-CTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915179_68915180insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915179_68915180insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682647_68682648insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682647_68682648insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439223_68439224insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16329_16330insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16329_16330insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+156_1041+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+156_259+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+156_201+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+156_201+157insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+156_201+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+156_201+157insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+162_195+163insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+162_195+163insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+156_299+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+156_956+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+156_*235+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+156_*235+157insATTTTTTTTTTTTTTTTTTTT...
ENST00000255078.7:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTT...
NM_002180.2:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_002171.2:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005273974.2:c.-100+156_-100+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+156_-100+157insATTTTTTTTTTTTTTTTTTTTTTT...
XM_005273976.1:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTT...
XR_247198.1:n.1014+156_1014+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+156_1014+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017669.2:c.-100+156_-100+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+156_-100+157insATTTTTTTTTTTTTTTTTTTTTTT...
XM_017017670.2:c.-100+156_-100+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+156_-100+157insATTTTTTTTTTTTTTTTTTTTTTT...
XM_017017671.2:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873160.1:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTT...
XR_949903.3:n.1010+156_1010+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+156_912+157insATTTTTTTTTTTTTTTTTTTTTTTTTTTT...