Canonical Allele Identifier: CA381653828

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1401871819
• gnomAD v2: 11-68704464-A-G
• gnomAD v4: 11-68936996-A-G
• MyVariant Identifiers: chr11:g.68704464A>G (hg19) ; chr11:g.68936996A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936996A>G , CM000673.2:g.68936996A>G	GRCh38
NC_000011.9:g.68704464A>G , CM000673.1:g.68704464A>G	GRCh37
NC_000011.8:g.68461040A>G	NCBI36
NG_007976.1:g.38146A>G , LRG_250:g.38146A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2516A>G MANE Select	ENSP00000255078.4:p.Gln839Arg
ENST00000674675.1:c.661A>G
ENST00000674878.1:c.621A>G
ENST00000675118.1:c.2004A>G
ENST00000675389.1:n.791A>G
ENST00000675615.1:c.2516A>G	ENSP00000502413.1:p.Gln839Arg
ENST00000675648.1:n.1891A>G
ENST00000675916.1:c.760A>G
ENST00000676173.1:n.3261A>G
ENST00000676182.1:c.947A>G
ENST00000676228.1:c.*1839A>G	ENSP00000502375.1:n.*1839A>G
ENST00000255078.7:c.2516A>G	ENSP00000255078.3:p.Gln839Arg
ENST00000539064.5:n.2275A>G
ENST00000543739.5:n.1509A>G
NM_002180.2:c.2516A>G , LRG_250t1:c.2516A>G	NP_002171.2:p.Gln839Arg
XM_005273974.2:c.1505A>G	XP_005274031.1:p.Gln502Arg
XM_005273975.2:c.1388A>G	XP_005274032.1:p.Gln463Arg
XM_011544994.1:c.1283A>G	XP_011543296.1:p.Gln428Arg
XR_949903.1:n.2618A>G
XM_005273975.3:c.1388A>G	XP_005274032.1:p.Gln463Arg
XM_017017669.2:c.1505A>G	XP_016873158.1:p.Gln502Arg
XM_017017670.2:c.1505A>G	XP_016873159.1:p.Gln502Arg
XR_949903.3:n.2614A>G
NM_002180.3:c.2516A>G MANE Select	NP_002171.2:p.Gln839Arg