Canonical Allele Identifier: CA475204512

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704432T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936964T>G , CM000673.2:g.68936964T>G	GRCh38
NC_000011.9:g.68704432T>G , CM000673.1:g.68704432T>G	GRCh37
NC_000011.8:g.68461008T>G	NCBI36
NG_007976.1:g.38114T>G , LRG_250:g.38114T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2484T>G MANE Select	ENSP00000255078.4:p.Pro828=
ENST00000674675.1:c.629T>G
ENST00000674878.1:c.589T>G
ENST00000675118.1:c.1972T>G
ENST00000675389.1:n.759T>G
ENST00000675615.1:c.2484T>G	ENSP00000502413.1:p.Pro828=
ENST00000675648.1:n.1859T>G
ENST00000675916.1:c.728T>G
ENST00000676173.1:n.3229T>G
ENST00000676182.1:c.915T>G
ENST00000676228.1:c.*1807T>G	ENSP00000502375.1:n.*1807T>G
ENST00000255078.7:c.2484T>G	ENSP00000255078.3:p.Pro828=
ENST00000539064.5:n.2243T>G
ENST00000543739.5:n.1477T>G
NM_002180.2:c.2484T>G , LRG_250t1:c.2484T>G	NP_002171.2:p.Pro828=
XM_005273974.2:c.1473T>G	XP_005274031.1:p.Pro491=
XM_005273975.2:c.1356T>G	XP_005274032.1:p.Pro452=
XM_011544994.1:c.1251T>G	XP_011543296.1:p.Pro417=
XR_949903.1:n.2586T>G
XM_005273975.3:c.1356T>G	XP_005274032.1:p.Pro452=
XM_017017669.2:c.1473T>G	XP_016873158.1:p.Pro491=
XM_017017670.2:c.1473T>G	XP_016873159.1:p.Pro491=
XR_949903.3:n.2582T>G
NM_002180.3:c.2484T>G MANE Select	NP_002171.2:p.Pro828=