Canonical Allele Identifier: CA475204538

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704459A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936991A>G , CM000673.2:g.68936991A>G	GRCh38
NC_000011.9:g.68704459A>G , CM000673.1:g.68704459A>G	GRCh37
NC_000011.8:g.68461035A>G	NCBI36
NG_007976.1:g.38141A>G , LRG_250:g.38141A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2511A>G MANE Select	ENSP00000255078.4:p.Arg837=
ENST00000674675.1:c.656A>G
ENST00000674878.1:c.616A>G
ENST00000675118.1:c.1999A>G
ENST00000675389.1:n.786A>G
ENST00000675615.1:c.2511A>G	ENSP00000502413.1:p.Arg837=
ENST00000675648.1:n.1886A>G
ENST00000675916.1:c.755A>G
ENST00000676173.1:n.3256A>G
ENST00000676182.1:c.942A>G
ENST00000676228.1:c.*1834A>G	ENSP00000502375.1:n.*1834A>G
ENST00000255078.7:c.2511A>G	ENSP00000255078.3:p.Arg837=
ENST00000539064.5:n.2270A>G
ENST00000543739.5:n.1504A>G
NM_002180.2:c.2511A>G , LRG_250t1:c.2511A>G	NP_002171.2:p.Arg837=
XM_005273974.2:c.1500A>G	XP_005274031.1:p.Arg500=
XM_005273975.2:c.1383A>G	XP_005274032.1:p.Arg461=
XM_011544994.1:c.1278A>G	XP_011543296.1:p.Arg426=
XR_949903.1:n.2613A>G
XM_005273975.3:c.1383A>G	XP_005274032.1:p.Arg461=
XM_017017669.2:c.1500A>G	XP_016873158.1:p.Arg500=
XM_017017670.2:c.1500A>G	XP_016873159.1:p.Arg500=
XR_949903.3:n.2609A>G
NM_002180.3:c.2511A>G MANE Select	NP_002171.2:p.Arg837=