Canonical Allele Identifier: CA2497320959

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1858273677
• gnomAD v3: 11-68908091-A-ATC
• gnomAD v4: 11-68908091-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908092_68908093insCT , CM000673.2:g.68908092_68908093insCT	GRCh38
NC_000011.9:g.68675560_68675561insCT , CM000673.1:g.68675560_68675561insCT	GRCh37
NC_000011.8:g.68432136_68432137insCT	NCBI36
NG_007976.1:g.9242_9243insCT , LRG_250:g.9242_9243insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.257-53_257-52insCT MANE Select	ENSP00000255078.4:n.257-53_257-52insCT
ENST00000539224.2:c.220-53_220-52insCT
ENST00000674583.1:c.220-53_220-52insCT
ENST00000674597.1:c.68-53_68-52insCT
ENST00000674955.1:c.257-53_257-52insCT	ENSP00000502463.1:n.257-53_257-52insCT
ENST00000675142.1:n.220-53_220-52insCT
ENST00000675469.1:c.133-53_133-52insCT
ENST00000675615.1:c.257-53_257-52insCT	ENSP00000502413.1:n.257-53_257-52insCT
ENST00000675674.1:n.220-53_220-52insCT
ENST00000675873.1:c.220-53_220-52insCT
ENST00000676173.1:n.301-53_301-52insCT
ENST00000676228.1:c.257-53_257-52insCT	ENSP00000502375.1:n.257-53_257-52insCT
ENST00000255078.7:c.257-53_257-52insCT	ENSP00000255078.3:n.257-53_257-52insCT
ENST00000539224.1:c.257-53_257-52insCT	ENSP00000440465.1:n.257-53_257-52insCT
ENST00000544541.1:c.87-53_87-52insCT	ENSP00000443343.1:n.87-53_87-52insCT
ENST00000545146.1:c.*127-53_*127-52insCT	ENSP00000456366.1:n.*127-53_*127-52insCT
NM_002180.2:c.257-53_257-52insCT , LRG_250t1:c.257-53_257-52insCT	NP_002171.2:n.257-53_257-52insCT
XM_005273974.2:c.-755-53_-755-52insCT	XP_005274031.1:n.-755-53_-755-52insCT
XM_005273976.1:c.257-53_257-52insCT	XP_005274033.1:n.257-53_257-52insCT
XR_247198.1:n.359-53_359-52insCT
XR_949903.1:n.359-53_359-52insCT
XM_005273976.2:c.257-53_257-52insCT	XP_005274033.1:n.257-53_257-52insCT
XM_017017669.2:c.-657-53_-657-52insCT	XP_016873158.1:n.-657-53_-657-52insCT
XM_017017671.2:c.257-53_257-52insCT	XP_016873160.1:n.257-53_257-52insCT
XR_949903.3:n.355-53_355-52insCT
NM_002180.3:c.257-53_257-52insCT MANE Select	NP_002171.2:n.257-53_257-52insCT