Canonical Allele Identifier: CA475192642

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68682377A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914909A>T , CM000673.2:g.68914909A>T	GRCh38
NC_000011.9:g.68682377A>T , CM000673.1:g.68682377A>T	GRCh37
NC_000011.8:g.68438953A>T	NCBI36
NG_007976.1:g.16059A>T , LRG_250:g.16059A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.798A>T MANE Select	ENSP00000255078.4:p.Gly266=
ENST00000539224.2:c.927A>T
ENST00000674955.1:c.798A>T	ENSP00000502463.1:p.Gly266=
ENST00000675118.1:c.145A>T
ENST00000675119.1:c.87A>T	ENSP00000501861.1:p.Gly29=
ENST00000675305.1:c.87A>T	ENSP00000502365.1:p.Gly29=
ENST00000675464.1:c.87A>T	ENSP00000502650.1:p.Gly29=
ENST00000675615.1:c.798A>T	ENSP00000502413.1:p.Gly266=
ENST00000675683.1:c.185A>T
ENST00000676173.1:n.842A>T
ENST00000676228.1:c.*121A>T	ENSP00000502375.1:n.*121A>T
ENST00000676239.1:n.112A>T
ENST00000255078.7:c.798A>T	ENSP00000255078.3:p.Gly266=
ENST00000539224.1:c.*121A>T	ENSP00000440465.1:n.*121A>T
NM_002180.2:c.798A>T , LRG_250t1:c.798A>T	NP_002171.2:p.Gly266=
XM_005273974.2:c.-214A>T	XP_005274031.1:n.-214A>T
XM_005273976.1:c.798A>T	XP_005274033.1:p.Gly266=
XR_247198.1:n.900A>T
XR_949903.1:n.900A>T
XM_005273976.2:c.798A>T	XP_005274033.1:p.Gly266=
XM_017017669.2:c.-214A>T	XP_016873158.1:n.-214A>T
XM_017017670.2:c.-214A>T	XP_016873159.1:n.-214A>T
XM_017017671.2:c.798A>T	XP_016873160.1:p.Gly266=
XR_949903.3:n.896A>T
NM_002180.3:c.798A>T MANE Select	NP_002171.2:p.Gly266=