Canonical Allele Identifier: CA939177904

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1858606674
• gnomAD v3: 11-68915166-C-CTTTTTTTTTTTTTTTTTTTGTTTTT
• gnomAD v4: 11-68915166-C-CTTTTTTTTTTTTTTTTTTTGTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915185_68915186insGTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915185_68915186insGTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682653_68682654insGTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682653_68682654insGTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439229_68439230insGTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16335_16336insGTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16335_16336insGTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+162_1041+163insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+162_259+163insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+162_201+163insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+162_201+163insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+162_201+163insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+162_201+163insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+168_195+169insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+168_195+169insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+162_299+163insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+162_956+163insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+162_*235+163insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+162_*235+163insGTTTTTTTTTTTTTTTTTTTT...
ENST00000255078.7:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTT...
NM_002180.2:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	NP_002171.2:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+162_-100+163insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+162_-100+163insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_005273976.1:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT
XR_247198.1:n.1014+162_1014+163insGTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+162_1014+163insGTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT
XM_017017669.2:c.-100+162_-100+163insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+162_-100+163insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017670.2:c.-100+162_-100+163insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+162_-100+163insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017671.2:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873160.1:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.3:n.1010+162_1010+163insGTTTTTTTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+162_912+163insGTTTTTTTTTTTTTTTTTTTTTTTT