Canonical Allele Identifier: CA381653004

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704143T>G (hg19) ; chr11:g.68936675T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936675T>G , CM000673.2:g.68936675T>G	GRCh38
NC_000011.9:g.68704143T>G , CM000673.1:g.68704143T>G	GRCh37
NC_000011.8:g.68460719T>G	NCBI36
NG_007976.1:g.37825T>G , LRG_250:g.37825T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2195T>G MANE Select	ENSP00000255078.4:p.Met732Arg
ENST00000674675.1:c.439T>G
ENST00000674878.1:c.439T>G
ENST00000674955.1:c.*912T>G	ENSP00000502463.1:n.*912T>G
ENST00000675118.1:c.1683T>G
ENST00000675389.1:n.470T>G
ENST00000675615.1:c.2195T>G	ENSP00000502413.1:p.Met732Arg
ENST00000675648.1:n.1570T>G
ENST00000675916.1:c.439T>G
ENST00000676173.1:n.2940T>G
ENST00000676182.1:c.626T>G
ENST00000676228.1:c.*1518T>G	ENSP00000502375.1:n.*1518T>G
ENST00000255078.7:c.2195T>G	ENSP00000255078.3:p.Met732Arg
ENST00000539064.5:n.1954T>G
ENST00000543739.5:n.1188T>G
NM_002180.2:c.2195T>G , LRG_250t1:c.2195T>G	NP_002171.2:p.Met732Arg
XM_005273974.2:c.1184T>G	XP_005274031.1:p.Met395Arg
XM_005273975.2:c.1067T>G	XP_005274032.1:p.Met356Arg
XM_011544994.1:c.962T>G	XP_011543296.1:p.Met321Arg
XR_949903.1:n.2297T>G
XM_005273975.3:c.1067T>G	XP_005274032.1:p.Met356Arg
XM_017017669.2:c.1184T>G	XP_016873158.1:p.Met395Arg
XM_017017670.2:c.1184T>G	XP_016873159.1:p.Met395Arg
XR_949903.3:n.2293T>G
NM_002180.3:c.2195T>G MANE Select	NP_002171.2:p.Met732Arg