Canonical Allele Identifier: CA381653858

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704473G>T (hg19) ; chr11:g.68937005G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937005G>T , CM000673.2:g.68937005G>T	GRCh38
NC_000011.9:g.68704473G>T , CM000673.1:g.68704473G>T	GRCh37
NC_000011.8:g.68461049G>T	NCBI36
NG_007976.1:g.38155G>T , LRG_250:g.38155G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2525G>T MANE Select	ENSP00000255078.4:p.Arg842Met
ENST00000674675.1:c.670G>T
ENST00000674878.1:c.630G>T
ENST00000675118.1:c.2013G>T
ENST00000675389.1:n.800G>T
ENST00000675615.1:c.2525G>T	ENSP00000502413.1:p.Arg842Met
ENST00000675648.1:n.1900G>T
ENST00000675916.1:c.769G>T
ENST00000676173.1:n.3270G>T
ENST00000676182.1:c.956G>T
ENST00000676228.1:c.*1848G>T	ENSP00000502375.1:n.*1848G>T
ENST00000255078.7:c.2525G>T	ENSP00000255078.3:p.Arg842Met
ENST00000539064.5:n.2284G>T
ENST00000543739.5:n.1518G>T
NM_002180.2:c.2525G>T , LRG_250t1:c.2525G>T	NP_002171.2:p.Arg842Met
XM_005273974.2:c.1514G>T	XP_005274031.1:p.Arg505Met
XM_005273975.2:c.1397G>T	XP_005274032.1:p.Arg466Met
XM_011544994.1:c.1292G>T	XP_011543296.1:p.Arg431Met
XR_949903.1:n.2627G>T
XM_005273975.3:c.1397G>T	XP_005274032.1:p.Arg466Met
XM_017017669.2:c.1514G>T	XP_016873158.1:p.Arg505Met
XM_017017670.2:c.1514G>T	XP_016873159.1:p.Arg505Met
XR_949903.3:n.2623G>T
NM_002180.3:c.2525G>T MANE Select	NP_002171.2:p.Arg842Met