Canonical Allele Identifier: CA939178669

Gene: IGHMBP2

Linked Data

• gnomAD v3: 11-68915204-A-ATTTTATT
• gnomAD v4: 11-68915204-A-ATTTTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915204_68915205insTTTTATT , CM000673.2:g.68915204_68915205insTTTTATT	GRCh38
NC_000011.9:g.68682672_68682673insTTTTATT , CM000673.1:g.68682672_68682673insTTTTATT	GRCh37
NC_000011.8:g.68439248_68439249insTTTTATT	NCBI36
NG_007976.1:g.16354_16355insTTTTATT , LRG_250:g.16354_16355insTTTTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+181_912+182insTTTTATT MANE Select	ENSP00000255078.4:n.912+181_912+182insTTTTATT
ENST00000539224.2:c.1041+181_1041+182insTTTTATT
ENST00000674955.1:c.912+181_912+182insTTTTATT	ENSP00000502463.1:n.912+181_912+182insTTTTATT
ENST00000675118.1:c.259+181_259+182insTTTTATT
ENST00000675119.1:c.201+181_201+182insTTTTATT	ENSP00000501861.1:n.201+181_201+182insTTTTATT
ENST00000675305.1:c.201+181_201+182insTTTTATT	ENSP00000502365.1:n.201+181_201+182insTTTTATT
ENST00000675464.1:c.195+187_195+188insTTTTATT	ENSP00000502650.1:n.195+187_195+188insTTTTATT
ENST00000675615.1:c.912+181_912+182insTTTTATT	ENSP00000502413.1:n.912+181_912+182insTTTTATT
ENST00000675683.1:c.299+181_299+182insTTTTATT
ENST00000676173.1:n.956+181_956+182insTTTTATT
ENST00000676228.1:c.*235+181_*235+182insTTTTATT	ENSP00000502375.1:n.*235+181_*235+182insTTTTATT
ENST00000255078.7:c.912+181_912+182insTTTTATT	ENSP00000255078.3:n.912+181_912+182insTTTTATT
NM_002180.2:c.912+181_912+182insTTTTATT , LRG_250t1:c.912+181_912+182insTTTTATT	NP_002171.2:n.912+181_912+182insTTTTATT
XM_005273974.2:c.-100+181_-100+182insTTTTATT	XP_005274031.1:n.-100+181_-100+182insTTTTATT
XM_005273976.1:c.912+181_912+182insTTTTATT	XP_005274033.1:n.912+181_912+182insTTTTATT
XR_247198.1:n.1014+181_1014+182insTTTTATT
XR_949903.1:n.1014+181_1014+182insTTTTATT
XM_005273976.2:c.912+181_912+182insTTTTATT	XP_005274033.1:n.912+181_912+182insTTTTATT
XM_017017669.2:c.-100+181_-100+182insTTTTATT	XP_016873158.1:n.-100+181_-100+182insTTTTATT
XM_017017670.2:c.-100+181_-100+182insTTTTATT	XP_016873159.1:n.-100+181_-100+182insTTTTATT
XM_017017671.2:c.912+181_912+182insTTTTATT	XP_016873160.1:n.912+181_912+182insTTTTATT
XR_949903.3:n.1010+181_1010+182insTTTTATT
NM_002180.3:c.912+181_912+182insTTTTATT MANE Select	NP_002171.2:n.912+181_912+182insTTTTATT