Canonical Allele Identifier: CA2614746366

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68915166-C-CTGTTTTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915167_68915168insGTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915167_68915168insGTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682635_68682636insGTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682635_68682636insGTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439211_68439212insGTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16317_16318insGTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16317_16318insGTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+144_1041+145insGTTTTTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+144_259+145insGTTTTTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+144_201+145insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+144_201+145insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+144_201+145insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+144_201+145insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+150_195+151insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+150_195+151insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+144_299+145insGTTTTTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+144_956+145insGTTTTTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+144_*235+145insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+144_*235+145insGTTTTTTTTTTTTTTTTTTTT...
ENST00000255078.7:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT...
NM_002180.2:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	NP_002171.2:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+144_-100+145insGTTTTTTTTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+144_-100+145insGTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.1:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT
XR_247198.1:n.1014+144_1014+145insGTTTTTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+144_1014+145insGTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT
XM_017017669.2:c.-100+144_-100+145insGTTTTTTTTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+144_-100+145insGTTTTTTTTTTTTTTTTTTTTTT
XM_017017670.2:c.-100+144_-100+145insGTTTTTTTTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+144_-100+145insGTTTTTTTTTTTTTTTTTTTTTT
XM_017017671.2:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT	XP_016873160.1:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT
XR_949903.3:n.1010+144_1010+145insGTTTTTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+144_912+145insGTTTTTTTTTTTTTTTTTTTTTT