Canonical Allele Identifier: CA381653851

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704470T>G (hg19) ; chr11:g.68937002T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937002T>G , CM000673.2:g.68937002T>G	GRCh38
NC_000011.9:g.68704470T>G , CM000673.1:g.68704470T>G	GRCh37
NC_000011.8:g.68461046T>G	NCBI36
NG_007976.1:g.38152T>G , LRG_250:g.38152T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2522T>G MANE Select	ENSP00000255078.4:p.Val841Gly
ENST00000674675.1:c.667T>G
ENST00000674878.1:c.627T>G
ENST00000675118.1:c.2010T>G
ENST00000675389.1:n.797T>G
ENST00000675615.1:c.2522T>G	ENSP00000502413.1:p.Val841Gly
ENST00000675648.1:n.1897T>G
ENST00000675916.1:c.766T>G
ENST00000676173.1:n.3267T>G
ENST00000676182.1:c.953T>G
ENST00000676228.1:c.*1845T>G	ENSP00000502375.1:n.*1845T>G
ENST00000255078.7:c.2522T>G	ENSP00000255078.3:p.Val841Gly
ENST00000539064.5:n.2281T>G
ENST00000543739.5:n.1515T>G
NM_002180.2:c.2522T>G , LRG_250t1:c.2522T>G	NP_002171.2:p.Val841Gly
XM_005273974.2:c.1511T>G	XP_005274031.1:p.Val504Gly
XM_005273975.2:c.1394T>G	XP_005274032.1:p.Val465Gly
XM_011544994.1:c.1289T>G	XP_011543296.1:p.Val430Gly
XR_949903.1:n.2624T>G
XM_005273975.3:c.1394T>G	XP_005274032.1:p.Val465Gly
XM_017017669.2:c.1511T>G	XP_016873158.1:p.Val504Gly
XM_017017670.2:c.1511T>G	XP_016873159.1:p.Val504Gly
XR_949903.3:n.2620T>G
NM_002180.3:c.2522T>G MANE Select	NP_002171.2:p.Val841Gly