Canonical Allele Identifier: CA2614746085

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68915130-G-GTCGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915133_68915137dup , CM000673.2:g.68915133_68915137dup	GRCh38
NC_000011.9:g.68682601_68682605dup , CM000673.1:g.68682601_68682605dup	GRCh37
NC_000011.8:g.68439177_68439181dup	NCBI36
NG_007976.1:g.16283_16287dup , LRG_250:g.16283_16287dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+110_912+114dup MANE Select	ENSP00000255078.4:n.912+110_912+114dup
ENST00000539224.2:c.1041+110_1041+114dup
ENST00000674955.1:c.912+110_912+114dup	ENSP00000502463.1:n.912+110_912+114dup
ENST00000675118.1:c.259+110_259+114dup
ENST00000675119.1:c.201+110_201+114dup	ENSP00000501861.1:n.201+110_201+114dup
ENST00000675305.1:c.201+110_201+114dup	ENSP00000502365.1:n.201+110_201+114dup
ENST00000675464.1:c.195+116_195+120dup	ENSP00000502650.1:n.195+116_195+120dup
ENST00000675615.1:c.912+110_912+114dup	ENSP00000502413.1:n.912+110_912+114dup
ENST00000675683.1:c.299+110_299+114dup
ENST00000676173.1:n.956+110_956+114dup
ENST00000676228.1:c.*235+110_*235+114dup	ENSP00000502375.1:n.*235+110_*235+114dup
ENST00000255078.7:c.912+110_912+114dup	ENSP00000255078.3:n.912+110_912+114dup
NM_002180.2:c.912+110_912+114dup , LRG_250t1:c.912+110_912+114dup	NP_002171.2:n.912+110_912+114dup
XM_005273974.2:c.-100+110_-100+114dup	XP_005274031.1:n.-100+110_-100+114dup
XM_005273976.1:c.912+110_912+114dup	XP_005274033.1:n.912+110_912+114dup
XR_247198.1:n.1014+110_1014+114dup
XR_949903.1:n.1014+110_1014+114dup
XM_005273976.2:c.912+110_912+114dup	XP_005274033.1:n.912+110_912+114dup
XM_017017669.2:c.-100+110_-100+114dup	XP_016873158.1:n.-100+110_-100+114dup
XM_017017670.2:c.-100+110_-100+114dup	XP_016873159.1:n.-100+110_-100+114dup
XM_017017671.2:c.912+110_912+114dup	XP_016873160.1:n.912+110_912+114dup
XR_949903.3:n.1010+110_1010+114dup
NM_002180.3:c.912+110_912+114dup MANE Select	NP_002171.2:n.912+110_912+114dup