Canonical Allele Identifier: CA381652481

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703894A>T (hg19) ; chr11:g.68936426A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936426A>T , CM000673.2:g.68936426A>T	GRCh38
NC_000011.9:g.68703894A>T , CM000673.1:g.68703894A>T	GRCh37
NC_000011.8:g.68460470A>T	NCBI36
NG_007976.1:g.37576A>T , LRG_250:g.37576A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.1946A>T MANE Select	ENSP00000255078.4:p.Glu649Val
ENST00000674675.1:c.190A>T
ENST00000674878.1:c.190A>T
ENST00000674955.1:c.*663A>T	ENSP00000502463.1:n.*663A>T
ENST00000675118.1:c.1434A>T
ENST00000675389.1:n.221A>T
ENST00000675615.1:c.1946A>T	ENSP00000502413.1:p.Glu649Val
ENST00000675648.1:n.1321A>T
ENST00000675916.1:c.190A>T
ENST00000676173.1:n.2691A>T
ENST00000676182.1:c.377A>T
ENST00000676228.1:c.*1269A>T	ENSP00000502375.1:n.*1269A>T
ENST00000255078.7:c.1946A>T	ENSP00000255078.3:p.Glu649Val
ENST00000539064.5:n.1705A>T
ENST00000543739.5:n.939A>T
ENST00000545475.1:n.542A>T
NM_002180.2:c.1946A>T , LRG_250t1:c.1946A>T	NP_002171.2:p.Glu649Val
XM_005273974.2:c.935A>T	XP_005274031.1:p.Glu312Val
XM_005273975.2:c.818A>T	XP_005274032.1:p.Glu273Val
XM_011544994.1:c.713A>T	XP_011543296.1:p.Glu238Val
XR_949903.1:n.2048A>T
XM_005273975.3:c.818A>T	XP_005274032.1:p.Glu273Val
XM_017017669.2:c.935A>T	XP_016873158.1:p.Glu312Val
XM_017017670.2:c.935A>T	XP_016873159.1:p.Glu312Val
XR_949903.3:n.2044A>T
NM_002180.3:c.1946A>T MANE Select	NP_002171.2:p.Glu649Val