Canonical Allele Identifier: CA381653733

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704419G>T (hg19) ; chr11:g.68936951G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936951G>T , CM000673.2:g.68936951G>T	GRCh38
NC_000011.9:g.68704419G>T , CM000673.1:g.68704419G>T	GRCh37
NC_000011.8:g.68460995G>T	NCBI36
NG_007976.1:g.38101G>T , LRG_250:g.38101G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2471G>T MANE Select	ENSP00000255078.4:p.Gly824Val
ENST00000674675.1:c.616G>T
ENST00000674878.1:c.576G>T
ENST00000675118.1:c.1959G>T
ENST00000675389.1:n.746G>T
ENST00000675615.1:c.2471G>T	ENSP00000502413.1:p.Gly824Val
ENST00000675648.1:n.1846G>T
ENST00000675916.1:c.715G>T
ENST00000676173.1:n.3216G>T
ENST00000676182.1:c.902G>T
ENST00000676228.1:c.*1794G>T	ENSP00000502375.1:n.*1794G>T
ENST00000255078.7:c.2471G>T	ENSP00000255078.3:p.Gly824Val
ENST00000539064.5:n.2230G>T
ENST00000543739.5:n.1464G>T
NM_002180.2:c.2471G>T , LRG_250t1:c.2471G>T	NP_002171.2:p.Gly824Val
XM_005273974.2:c.1460G>T	XP_005274031.1:p.Gly487Val
XM_005273975.2:c.1343G>T	XP_005274032.1:p.Gly448Val
XM_011544994.1:c.1238G>T	XP_011543296.1:p.Gly413Val
XR_949903.1:n.2573G>T
XM_005273975.3:c.1343G>T	XP_005274032.1:p.Gly448Val
XM_017017669.2:c.1460G>T	XP_016873158.1:p.Gly487Val
XM_017017670.2:c.1460G>T	XP_016873159.1:p.Gly487Val
XR_949903.3:n.2569G>T
NM_002180.3:c.2471G>T MANE Select	NP_002171.2:p.Gly824Val