Canonical Allele Identifier: CA381653531

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704353C>G (hg19) ; chr11:g.68936885C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936885C>G , CM000673.2:g.68936885C>G	GRCh38
NC_000011.9:g.68704353C>G , CM000673.1:g.68704353C>G	GRCh37
NC_000011.8:g.68460929C>G	NCBI36
NG_007976.1:g.38035C>G , LRG_250:g.38035C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2405C>G MANE Select	ENSP00000255078.4:p.Pro802Arg
ENST00000674675.1:c.588-38C>G
ENST00000674878.1:c.548-38C>G
ENST00000675118.1:c.1893C>G
ENST00000675389.1:n.680C>G
ENST00000675615.1:c.2405C>G	ENSP00000502413.1:p.Pro802Arg
ENST00000675648.1:n.1780C>G
ENST00000675916.1:c.649C>G
ENST00000676173.1:n.3150C>G
ENST00000676182.1:c.836C>G
ENST00000676228.1:c.*1728C>G	ENSP00000502375.1:n.*1728C>G
ENST00000255078.7:c.2405C>G	ENSP00000255078.3:p.Pro802Arg
ENST00000539064.5:n.2164C>G
ENST00000543739.5:n.1398C>G
NM_002180.2:c.2405C>G , LRG_250t1:c.2405C>G	NP_002171.2:p.Pro802Arg
XM_005273974.2:c.1394C>G	XP_005274031.1:p.Pro465Arg
XM_005273975.2:c.1277C>G	XP_005274032.1:p.Pro426Arg
XM_011544994.1:c.1172C>G	XP_011543296.1:p.Pro391Arg
XR_949903.1:n.2507C>G
XM_005273975.3:c.1277C>G	XP_005274032.1:p.Pro426Arg
XM_017017669.2:c.1394C>G	XP_016873158.1:p.Pro465Arg
XM_017017670.2:c.1394C>G	XP_016873159.1:p.Pro465Arg
XR_949903.3:n.2503C>G
NM_002180.3:c.2405C>G MANE Select	NP_002171.2:p.Pro802Arg