Canonical Allele Identifier: CA381653617

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs2154008913
• MyVariant Identifiers: chr11:g.68704380C>G (hg19) ; chr11:g.68936912C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936912C>G , CM000673.2:g.68936912C>G	GRCh38
NC_000011.9:g.68704380C>G , CM000673.1:g.68704380C>G	GRCh37
NC_000011.8:g.68460956C>G	NCBI36
NG_007976.1:g.38062C>G , LRG_250:g.38062C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2432C>G MANE Select	ENSP00000255078.4:p.Thr811Ser
ENST00000674675.1:c.588-11C>G
ENST00000674878.1:c.548-11C>G
ENST00000675118.1:c.1920C>G
ENST00000675389.1:n.707C>G
ENST00000675615.1:c.2432C>G	ENSP00000502413.1:p.Thr811Ser
ENST00000675648.1:n.1807C>G
ENST00000675916.1:c.676C>G
ENST00000676173.1:n.3177C>G
ENST00000676182.1:c.863C>G
ENST00000676228.1:c.*1755C>G	ENSP00000502375.1:n.*1755C>G
ENST00000255078.7:c.2432C>G	ENSP00000255078.3:p.Thr811Ser
ENST00000539064.5:n.2191C>G
ENST00000543739.5:n.1425C>G
NM_002180.2:c.2432C>G , LRG_250t1:c.2432C>G	NP_002171.2:p.Thr811Ser
XM_005273974.2:c.1421C>G	XP_005274031.1:p.Thr474Ser
XM_005273975.2:c.1304C>G	XP_005274032.1:p.Thr435Ser
XM_011544994.1:c.1199C>G	XP_011543296.1:p.Thr400Ser
XR_949903.1:n.2534C>G
XM_005273975.3:c.1304C>G	XP_005274032.1:p.Thr435Ser
XM_017017669.2:c.1421C>G	XP_016873158.1:p.Thr474Ser
XM_017017670.2:c.1421C>G	XP_016873159.1:p.Thr474Ser
XR_949903.3:n.2530C>G
NM_002180.3:c.2432C>G MANE Select	NP_002171.2:p.Thr811Ser