Canonical Allele Identifier: CA475204329

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703778C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936310C>G , CM000673.2:g.68936310C>G	GRCh38
NC_000011.9:g.68703778C>G , CM000673.1:g.68703778C>G	GRCh37
NC_000011.8:g.68460354C>G	NCBI36
NG_007976.1:g.37460C>G , LRG_250:g.37460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1830C>G MANE Select	ENSP00000255078.4:p.Val610=
ENST00000674675.1:c.74C>G
ENST00000674878.1:c.74C>G
ENST00000674955.1:c.*547C>G	ENSP00000502463.1:n.*547C>G
ENST00000675118.1:c.1318C>G
ENST00000675389.1:n.105C>G
ENST00000675615.1:c.1830C>G	ENSP00000502413.1:p.Val610=
ENST00000675648.1:n.1205C>G
ENST00000675916.1:c.74C>G
ENST00000676173.1:n.2575C>G
ENST00000676182.1:c.261C>G
ENST00000676228.1:c.*1153C>G	ENSP00000502375.1:n.*1153C>G
ENST00000255078.7:c.1830C>G	ENSP00000255078.3:p.Val610=
ENST00000539064.5:n.1589C>G
ENST00000541229.5:n.525C>G
ENST00000543739.5:n.823C>G
ENST00000545475.1:n.426C>G
NM_002180.2:c.1830C>G , LRG_250t1:c.1830C>G	NP_002171.2:p.Val610=
XM_005273974.2:c.819C>G	XP_005274031.1:p.Val273=
XM_005273975.2:c.702C>G	XP_005274032.1:p.Val234=
XM_011544994.1:c.597C>G	XP_011543296.1:p.Val199=
XR_949903.1:n.1932C>G
XM_005273975.3:c.702C>G	XP_005274032.1:p.Val234=
XM_017017669.2:c.819C>G	XP_016873158.1:p.Val273=
XM_017017670.2:c.819C>G	XP_016873159.1:p.Val273=
XR_949903.3:n.1928C>G
NM_002180.3:c.1830C>G MANE Select	NP_002171.2:p.Val610=