Canonical Allele Identifier: CA475278959

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703895A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936427A>G , CM000673.2:g.68936427A>G	GRCh38
NC_000011.9:g.68703895A>G , CM000673.1:g.68703895A>G	GRCh37
NC_000011.8:g.68460471A>G	NCBI36
NG_007976.1:g.37577A>G , LRG_250:g.37577A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.1947A>G MANE Select	ENSP00000255078.4:p.Glu649=
ENST00000674675.1:c.191A>G
ENST00000674878.1:c.191A>G
ENST00000674955.1:c.*664A>G	ENSP00000502463.1:n.*664A>G
ENST00000675118.1:c.1435A>G
ENST00000675389.1:n.222A>G
ENST00000675615.1:c.1947A>G	ENSP00000502413.1:p.Glu649=
ENST00000675648.1:n.1322A>G
ENST00000675916.1:c.191A>G
ENST00000676173.1:n.2692A>G
ENST00000676182.1:c.378A>G
ENST00000676228.1:c.*1270A>G	ENSP00000502375.1:n.*1270A>G
ENST00000255078.7:c.1947A>G	ENSP00000255078.3:p.Glu649=
ENST00000539064.5:n.1706A>G
ENST00000543739.5:n.940A>G
ENST00000545475.1:n.543A>G
NM_002180.2:c.1947A>G , LRG_250t1:c.1947A>G	NP_002171.2:p.Glu649=
XM_005273974.2:c.936A>G	XP_005274031.1:p.Glu312=
XM_005273975.2:c.819A>G	XP_005274032.1:p.Glu273=
XM_011544994.1:c.714A>G	XP_011543296.1:p.Glu238=
XR_949903.1:n.2049A>G
XM_005273975.3:c.819A>G	XP_005274032.1:p.Glu273=
XM_017017669.2:c.936A>G	XP_016873158.1:p.Glu312=
XM_017017670.2:c.936A>G	XP_016873159.1:p.Glu312=
XR_949903.3:n.2045A>G
NM_002180.3:c.1947A>G MANE Select	NP_002171.2:p.Glu649=