Canonical Allele Identifier: CA2614746219

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68908138-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908138T>A , CM000673.2:g.68908138T>A	GRCh38
NC_000011.9:g.68675606T>A , CM000673.1:g.68675606T>A	GRCh37
NC_000011.8:g.68432182T>A	NCBI36
NG_007976.1:g.9288T>A , LRG_250:g.9288T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.257-7T>A MANE Select	ENSP00000255078.4:n.257-7T>A
ENST00000539224.2:c.220-7T>A
ENST00000674583.1:c.220-7T>A
ENST00000674597.1:c.68-7T>A
ENST00000674955.1:c.257-7T>A	ENSP00000502463.1:n.257-7T>A
ENST00000675142.1:n.220-7T>A
ENST00000675469.1:c.133-7T>A
ENST00000675615.1:c.257-7T>A	ENSP00000502413.1:n.257-7T>A
ENST00000675674.1:n.220-7T>A
ENST00000675873.1:c.220-7T>A
ENST00000676173.1:n.301-7T>A
ENST00000676228.1:c.257-7T>A	ENSP00000502375.1:n.257-7T>A
ENST00000255078.7:c.257-7T>A	ENSP00000255078.3:n.257-7T>A
ENST00000539224.1:c.257-7T>A	ENSP00000440465.1:n.257-7T>A
ENST00000544541.1:c.87-7T>A	ENSP00000443343.1:n.87-7T>A
ENST00000545146.1:c.*127-7T>A	ENSP00000456366.1:n.*127-7T>A
NM_002180.2:c.257-7T>A , LRG_250t1:c.257-7T>A	NP_002171.2:n.257-7T>A
XM_005273974.2:c.-755-7T>A	XP_005274031.1:n.-755-7T>A
XM_005273976.1:c.257-7T>A	XP_005274033.1:n.257-7T>A
XR_247198.1:n.359-7T>A
XR_949903.1:n.359-7T>A
XM_005273976.2:c.257-7T>A	XP_005274033.1:n.257-7T>A
XM_017017669.2:c.-657-7T>A	XP_016873158.1:n.-657-7T>A
XM_017017671.2:c.257-7T>A	XP_016873160.1:n.257-7T>A
XR_949903.3:n.355-7T>A
NM_002180.3:c.257-7T>A MANE Select	NP_002171.2:n.257-7T>A