Canonical Allele Identifier: CA2547263664

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915183_68915184insGTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915183_68915184insGTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000011.9:g.68682651_68682652insGTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682651_68682652insGTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000011.8:g.68439227_68439228insGTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_007976.1:g.16333_16334insGTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16333_16334insGTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000255078.4:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+160_1041+161insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502463.1:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+160_259+161insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+160_201+161insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000501861.1:n.201+160_201+161insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+160_201+161insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502365.1:n.201+160_201+161insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+166_195+167insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502650.1:n.195+166_195+167insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502413.1:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+160_299+161insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+160_956+161insGTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+160_*235+161insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000502375.1:n.*235+160_*235+161insGTTTTTTTTTTTTTTTTTTTT...
ENST00000255078.7:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000255078.3:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTT...
NM_002180.2:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	NP_002171.2:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+160_-100+161insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274031.1:n.-100+160_-100+161insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_005273976.1:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT
XR_247198.1:n.1014+160_1014+161insGTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+160_1014+161insGTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_005274033.1:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT
XM_017017669.2:c.-100+160_-100+161insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873158.1:n.-100+160_-100+161insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017670.2:c.-100+160_-100+161insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873159.1:n.-100+160_-100+161insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017671.2:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT	XP_016873160.1:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.3:n.1010+160_1010+161insGTTTTTTTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_002171.2:n.912+160_912+161insGTTTTTTTTTTTTTTTTTTTTTTTT