Canonical Allele Identifier: CA679620758

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1359509376
• MyVariant Identifiers: chr11:g.68676106A>G (hg19) ; chr11:g.68908638A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908638A>G , CM000673.2:g.68908638A>G	GRCh38
NC_000011.9:g.68676106A>G , CM000673.1:g.68676106A>G	GRCh37
NC_000011.8:g.68432682A>G	NCBI36
NG_007976.1:g.9788A>G , LRG_250:g.9788A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.547+7A>G MANE Select	ENSP00000255078.4:n.547+7A>G
ENST00000539224.2:c.510+7A>G
ENST00000674583.1:c.510+7A>G
ENST00000674955.1:c.547+7A>G	ENSP00000502463.1:n.547+7A>G
ENST00000675142.1:n.510+7A>G
ENST00000675615.1:c.547+7A>G	ENSP00000502413.1:n.547+7A>G
ENST00000675674.1:n.510+7A>G
ENST00000675683.1:c.98+7A>G
ENST00000675873.1:c.510+7A>G
ENST00000676173.1:n.591+7A>G
ENST00000676228.1:c.449+301A>G	ENSP00000502375.1:n.449+301A>G
ENST00000255078.7:c.547+7A>G	ENSP00000255078.3:n.547+7A>G
ENST00000539224.1:c.449+301A>G	ENSP00000440465.1:n.449+301A>G
ENST00000544541.1:c.*287+7A>G	ENSP00000443343.1:n.*287+7A>G
NM_002180.2:c.547+7A>G , LRG_250t1:c.547+7A>G	NP_002171.2:n.547+7A>G
XM_005273974.2:c.-465+7A>G	XP_005274031.1:n.-465+7A>G
XM_005273976.1:c.547+7A>G	XP_005274033.1:n.547+7A>G
XR_247198.1:n.649+7A>G
XR_949903.1:n.649+7A>G
XM_005273976.2:c.547+7A>G	XP_005274033.1:n.547+7A>G
XM_017017669.2:c.-465+301A>G	XP_016873158.1:n.-465+301A>G
XM_017017671.2:c.547+7A>G	XP_016873160.1:n.547+7A>G
XR_949903.3:n.645+7A>G
NM_002180.3:c.547+7A>G MANE Select	NP_002171.2:n.547+7A>G