Canonical Allele Identifier: CA381652043

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703880C>G (hg19) ; chr11:g.68936412C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936412C>G , CM000673.2:g.68936412C>G	GRCh38
NC_000011.9:g.68703880C>G , CM000673.1:g.68703880C>G	GRCh37
NC_000011.8:g.68460456C>G	NCBI36
NG_007976.1:g.37562C>G , LRG_250:g.37562C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1932C>G MANE Select	ENSP00000255078.4:p.Asp644Glu
ENST00000674675.1:c.176C>G
ENST00000674878.1:c.176C>G
ENST00000674955.1:c.*649C>G	ENSP00000502463.1:n.*649C>G
ENST00000675118.1:c.1420C>G
ENST00000675389.1:n.207C>G
ENST00000675615.1:c.1932C>G	ENSP00000502413.1:p.Asp644Glu
ENST00000675648.1:n.1307C>G
ENST00000675916.1:c.176C>G
ENST00000676173.1:n.2677C>G
ENST00000676182.1:c.363C>G
ENST00000676228.1:c.*1255C>G	ENSP00000502375.1:n.*1255C>G
ENST00000255078.7:c.1932C>G	ENSP00000255078.3:p.Asp644Glu
ENST00000539064.5:n.1691C>G
ENST00000543739.5:n.925C>G
ENST00000545475.1:n.528C>G
NM_002180.2:c.1932C>G , LRG_250t1:c.1932C>G	NP_002171.2:p.Asp644Glu
XM_005273974.2:c.921C>G	XP_005274031.1:p.Asp307Glu
XM_005273975.2:c.804C>G	XP_005274032.1:p.Asp268Glu
XM_011544994.1:c.699C>G	XP_011543296.1:p.Asp233Glu
XR_949903.1:n.2034C>G
XM_005273975.3:c.804C>G	XP_005274032.1:p.Asp268Glu
XM_017017669.2:c.921C>G	XP_016873158.1:p.Asp307Glu
XM_017017670.2:c.921C>G	XP_016873159.1:p.Asp307Glu
XR_949903.3:n.2030C>G
NM_002180.3:c.1932C>G MANE Select	NP_002171.2:p.Asp644Glu