Canonical Allele Identifier: CA381653183

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704221T>C (hg19) ; chr11:g.68936753T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936753T>C , CM000673.2:g.68936753T>C	GRCh38
NC_000011.9:g.68704221T>C , CM000673.1:g.68704221T>C	GRCh37
NC_000011.8:g.68460797T>C	NCBI36
NG_007976.1:g.37903T>C , LRG_250:g.37903T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2273T>C MANE Select	ENSP00000255078.4:p.Val758Ala
ENST00000674675.1:c.517T>C
ENST00000674878.1:c.517T>C
ENST00000674955.1:c.*990T>C	ENSP00000502463.1:n.*990T>C
ENST00000675118.1:c.1761T>C
ENST00000675389.1:n.548T>C
ENST00000675615.1:c.2273T>C	ENSP00000502413.1:p.Val758Ala
ENST00000675648.1:n.1648T>C
ENST00000675916.1:c.517T>C
ENST00000676173.1:n.3018T>C
ENST00000676182.1:c.704T>C
ENST00000676228.1:c.*1596T>C	ENSP00000502375.1:n.*1596T>C
ENST00000255078.7:c.2273T>C	ENSP00000255078.3:p.Val758Ala
ENST00000539064.5:n.2032T>C
ENST00000543739.5:n.1266T>C
NM_002180.2:c.2273T>C , LRG_250t1:c.2273T>C	NP_002171.2:p.Val758Ala
XM_005273974.2:c.1262T>C	XP_005274031.1:p.Val421Ala
XM_005273975.2:c.1145T>C	XP_005274032.1:p.Val382Ala
XM_011544994.1:c.1040T>C	XP_011543296.1:p.Val347Ala
XR_949903.1:n.2375T>C
XM_005273975.3:c.1145T>C	XP_005274032.1:p.Val382Ala
XM_017017669.2:c.1262T>C	XP_016873158.1:p.Val421Ala
XM_017017670.2:c.1262T>C	XP_016873159.1:p.Val421Ala
XR_949903.3:n.2371T>C
NM_002180.3:c.2273T>C MANE Select	NP_002171.2:p.Val758Ala