Canonical Allele Identifier: CA2614746373

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68915166-C-CTTTTTTGTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915172_68915173insGTTTTTTTTTTTTTTTTT , CM000673.2:g.68915172_68915173insGTTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682640_68682641insGTTTTTTTTTTTTTTTTT , CM000673.1:g.68682640_68682641insGTTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439216_68439217insGTTTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16322_16323insGTTTTTTTTTTTTTTTTT , LRG_250:g.16322_16323insGTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+149_912+150insGTTTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
ENST00000539224.2:c.1041+149_1041+150insGTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
ENST00000675118.1:c.259+149_259+150insGTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+149_201+150insGTTTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+149_201+150insGTTTTTTTTTTTTTTTTT
ENST00000675305.1:c.201+149_201+150insGTTTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+149_201+150insGTTTTTTTTTTTTTTTTT
ENST00000675464.1:c.195+155_195+156insGTTTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+155_195+156insGTTTTTTTTTTTTTTTTT
ENST00000675615.1:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
ENST00000675683.1:c.299+149_299+150insGTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+149_956+150insGTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+149_*235+150insGTTTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+149_*235+150insGTTTTTTTTTTTTTTTTT
ENST00000255078.7:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
NM_002180.2:c.912+149_912+150insGTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	NP_002171.2:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+149_-100+150insGTTTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+149_-100+150insGTTTTTTTTTTTTTTTTT
XM_005273976.1:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
XR_247198.1:n.1014+149_1014+150insGTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+149_1014+150insGTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
XM_017017669.2:c.-100+149_-100+150insGTTTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+149_-100+150insGTTTTTTTTTTTTTTTTT
XM_017017670.2:c.-100+149_-100+150insGTTTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+149_-100+150insGTTTTTTTTTTTTTTTTT
XM_017017671.2:c.912+149_912+150insGTTTTTTTTTTTTTTTTT	XP_016873160.1:n.912+149_912+150insGTTTTTTTTTTTTTTTTT
XR_949903.3:n.1010+149_1010+150insGTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+149_912+150insGTTTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+149_912+150insGTTTTTTTTTTTTTTTTT