Canonical Allele Identifier: CA6153436

Gene: IGHMBP2

Linked Data

• ClinVar Variation Id: 305839
• ClinVar RCV Id: RCV000398405
• dbSNP Id: rs758392980
• ExAC: 11:68682495 G / A
• gnomAD v2: 11-68682495-G-A
• gnomAD v4: 11-68915027-G-A
• MyVariant Identifiers: chr11:g.68682495G>A (hg19) ; chr11:g.68915027G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915027G>A , CM000673.2:g.68915027G>A	GRCh38
NC_000011.9:g.68682495G>A , CM000673.1:g.68682495G>A	GRCh37
NC_000011.8:g.68439071G>A	NCBI36
NG_007976.1:g.16177G>A , LRG_250:g.16177G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+4G>A MANE Select	ENSP00000255078.4:n.912+4G>A
ENST00000539224.2:c.1041+4G>A
ENST00000674955.1:c.912+4G>A	ENSP00000502463.1:n.912+4G>A
ENST00000675118.1:c.259+4G>A
ENST00000675119.1:c.201+4G>A	ENSP00000501861.1:n.201+4G>A
ENST00000675305.1:c.201+4G>A	ENSP00000502365.1:n.201+4G>A
ENST00000675464.1:c.195+10G>A	ENSP00000502650.1:n.195+10G>A
ENST00000675615.1:c.912+4G>A	ENSP00000502413.1:n.912+4G>A
ENST00000675683.1:c.299+4G>A
ENST00000676173.1:n.956+4G>A
ENST00000676228.1:c.*235+4G>A	ENSP00000502375.1:n.*235+4G>A
ENST00000255078.7:c.912+4G>A	ENSP00000255078.3:n.912+4G>A
NM_002180.2:c.912+4G>A , LRG_250t1:c.912+4G>A	NP_002171.2:n.912+4G>A
XM_005273974.2:c.-100+4G>A	XP_005274031.1:n.-100+4G>A
XM_005273976.1:c.912+4G>A	XP_005274033.1:n.912+4G>A
XR_247198.1:n.1014+4G>A
XR_949903.1:n.1014+4G>A
XM_005273976.2:c.912+4G>A	XP_005274033.1:n.912+4G>A
XM_017017669.2:c.-100+4G>A	XP_016873158.1:n.-100+4G>A
XM_017017670.2:c.-100+4G>A	XP_016873159.1:n.-100+4G>A
XM_017017671.2:c.912+4G>A	XP_016873160.1:n.912+4G>A
XR_949903.3:n.1010+4G>A
NM_002180.3:c.912+4G>A MANE Select	NP_002171.2:n.912+4G>A