Canonical Allele Identifier: CA381652638

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703968A>G (hg19) ; chr11:g.68936500A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936500A>G , CM000673.2:g.68936500A>G	GRCh38
NC_000011.9:g.68703968A>G , CM000673.1:g.68703968A>G	GRCh37
NC_000011.8:g.68460544A>G	NCBI36
NG_007976.1:g.37650A>G , LRG_250:g.37650A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2020A>G MANE Select	ENSP00000255078.4:p.Arg674Gly
ENST00000674675.1:c.264A>G
ENST00000674878.1:c.264A>G
ENST00000674955.1:c.*737A>G	ENSP00000502463.1:n.*737A>G
ENST00000675118.1:c.1508A>G
ENST00000675389.1:n.295A>G
ENST00000675615.1:c.2020A>G	ENSP00000502413.1:p.Arg674Gly
ENST00000675648.1:n.1395A>G
ENST00000675916.1:c.264A>G
ENST00000676173.1:n.2765A>G
ENST00000676182.1:c.451A>G
ENST00000676228.1:c.*1343A>G	ENSP00000502375.1:n.*1343A>G
ENST00000255078.7:c.2020A>G	ENSP00000255078.3:p.Arg674Gly
ENST00000539064.5:n.1779A>G
ENST00000543739.5:n.1013A>G
NM_002180.2:c.2020A>G , LRG_250t1:c.2020A>G	NP_002171.2:p.Arg674Gly
XM_005273974.2:c.1009A>G	XP_005274031.1:p.Arg337Gly
XM_005273975.2:c.892A>G	XP_005274032.1:p.Arg298Gly
XM_011544994.1:c.787A>G	XP_011543296.1:p.Arg263Gly
XR_949903.1:n.2122A>G
XM_005273975.3:c.892A>G	XP_005274032.1:p.Arg298Gly
XM_017017669.2:c.1009A>G	XP_016873158.1:p.Arg337Gly
XM_017017670.2:c.1009A>G	XP_016873159.1:p.Arg337Gly
XR_949903.3:n.2118A>G
NM_002180.3:c.2020A>G MANE Select	NP_002171.2:p.Arg674Gly