Canonical Allele Identifier: CA381651966

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703861C>G (hg19) ; chr11:g.68936393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936393C>G , CM000673.2:g.68936393C>G	GRCh38
NC_000011.9:g.68703861C>G , CM000673.1:g.68703861C>G	GRCh37
NC_000011.8:g.68460437C>G	NCBI36
NG_007976.1:g.37543C>G , LRG_250:g.37543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1913C>G MANE Select	ENSP00000255078.4:p.Thr638Arg
ENST00000674675.1:c.157C>G
ENST00000674878.1:c.157C>G
ENST00000674955.1:c.*630C>G	ENSP00000502463.1:n.*630C>G
ENST00000675118.1:c.1401C>G
ENST00000675389.1:n.188C>G
ENST00000675615.1:c.1913C>G	ENSP00000502413.1:p.Thr638Arg
ENST00000675648.1:n.1288C>G
ENST00000675916.1:c.157C>G
ENST00000676173.1:n.2658C>G
ENST00000676182.1:c.344C>G
ENST00000676228.1:c.*1236C>G	ENSP00000502375.1:n.*1236C>G
ENST00000255078.7:c.1913C>G	ENSP00000255078.3:p.Thr638Arg
ENST00000539064.5:n.1672C>G
ENST00000543739.5:n.906C>G
ENST00000545475.1:n.509C>G
NM_002180.2:c.1913C>G , LRG_250t1:c.1913C>G	NP_002171.2:p.Thr638Arg
XM_005273974.2:c.902C>G	XP_005274031.1:p.Thr301Arg
XM_005273975.2:c.785C>G	XP_005274032.1:p.Thr262Arg
XM_011544994.1:c.680C>G	XP_011543296.1:p.Thr227Arg
XR_949903.1:n.2015C>G
XM_005273975.3:c.785C>G	XP_005274032.1:p.Thr262Arg
XM_017017669.2:c.902C>G	XP_016873158.1:p.Thr301Arg
XM_017017670.2:c.902C>G	XP_016873159.1:p.Thr301Arg
XR_949903.3:n.2011C>G
NM_002180.3:c.1913C>G MANE Select	NP_002171.2:p.Thr638Arg