Canonical Allele Identifier: CA939178367

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1191505010
• gnomAD v3: 11-68915166-C-CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
• gnomAD v4: 11-68915166-C-CCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915166_68915167insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915166_68915167insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682634_68682635insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682634_68682635insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439210_68439211insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16316_16317insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16316_16317insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+143_1041+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+143_259+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+143_201+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+143_201+144insCTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+143_201+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+143_201+144insCTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+149_195+150insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+149_195+150insCTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+143_299+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+143_956+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+143_*235+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+143_*235+144insCTTTTTTTTTTTTTTTTTTTT...
ENST00000255078.7:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTT...
NM_002180.2:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_002171.2:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005273974.2:c.-100+143_-100+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+143_-100+144insCTTTTTTTTTTTTTTTTTTTTTTT...
XM_005273976.1:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTT...
XR_247198.1:n.1014+143_1014+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+143_1014+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017669.2:c.-100+143_-100+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+143_-100+144insCTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017670.2:c.-100+143_-100+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+143_-100+144insCTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017671.2:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873160.1:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTT...
XR_949903.3:n.1010+143_1010+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+143_912+144insCTTTTTTTTTTTTTTTTTTTTTTTTTTTT...