Canonical Allele Identifier: CA939178729

Gene: IGHMBP2

Linked Data

• gnomAD v3: 11-68915205-G-GTTTTTTTTTTTTTTT
• gnomAD v4: 11-68915205-G-GTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915209_68915210insTTTTTTTTTTTTTTT , CM000673.2:g.68915209_68915210insTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682677_68682678insTTTTTTTTTTTTTTT , CM000673.1:g.68682677_68682678insTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439253_68439254insTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16359_16360insTTTTTTTTTTTTTTT , LRG_250:g.16359_16360insTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+186_912+187insTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+186_912+187insTTTTTTTTTTTTTTT
ENST00000539224.2:c.1041+186_1041+187insTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+186_912+187insTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+186_912+187insTTTTTTTTTTTTTTT
ENST00000675118.1:c.259+186_259+187insTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+186_201+187insTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+186_201+187insTTTTTTTTTTTTTTT
ENST00000675305.1:c.201+186_201+187insTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+186_201+187insTTTTTTTTTTTTTTT
ENST00000675464.1:c.195+192_195+193insTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+192_195+193insTTTTTTTTTTTTTTT
ENST00000675615.1:c.912+186_912+187insTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+186_912+187insTTTTTTTTTTTTTTT
ENST00000675683.1:c.299+186_299+187insTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+186_956+187insTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+186_*235+187insTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+186_*235+187insTTTTTTTTTTTTTTT
ENST00000255078.7:c.912+186_912+187insTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+186_912+187insTTTTTTTTTTTTTTT
NM_002180.2:c.912+186_912+187insTTTTTTTTTTTTTTT , LRG_250t1:c.912+186_912+187insTTTTTTTTTTTTTTT	NP_002171.2:n.912+186_912+187insTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+186_-100+187insTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+186_-100+187insTTTTTTTTTTTTTTT
XM_005273976.1:c.912+186_912+187insTTTTTTTTTTTTTTT	XP_005274033.1:n.912+186_912+187insTTTTTTTTTTTTTTT
XR_247198.1:n.1014+186_1014+187insTTTTTTTTTTTTTTT
XR_949903.1:n.1014+186_1014+187insTTTTTTTTTTTTTTT
XM_005273976.2:c.912+186_912+187insTTTTTTTTTTTTTTT	XP_005274033.1:n.912+186_912+187insTTTTTTTTTTTTTTT
XM_017017669.2:c.-100+186_-100+187insTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+186_-100+187insTTTTTTTTTTTTTTT
XM_017017670.2:c.-100+186_-100+187insTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+186_-100+187insTTTTTTTTTTTTTTT
XM_017017671.2:c.912+186_912+187insTTTTTTTTTTTTTTT	XP_016873160.1:n.912+186_912+187insTTTTTTTTTTTTTTT
XR_949903.3:n.1010+186_1010+187insTTTTTTTTTTTTTTT
NM_002180.3:c.912+186_912+187insTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+186_912+187insTTTTTTTTTTTTTTT