Canonical Allele Identifier: CA475186049

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68675614T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908146T>C , CM000673.2:g.68908146T>C	GRCh38
NC_000011.9:g.68675614T>C , CM000673.1:g.68675614T>C	GRCh37
NC_000011.8:g.68432190T>C	NCBI36
NG_007976.1:g.9296T>C , LRG_250:g.9296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.258T>C MANE Select	ENSP00000255078.4:p.Gly86=
ENST00000539224.2:c.221T>C
ENST00000674583.1:c.221T>C
ENST00000674597.1:c.69T>C
ENST00000674955.1:c.258T>C	ENSP00000502463.1:p.Gly86=
ENST00000675142.1:n.221T>C
ENST00000675469.1:c.134T>C
ENST00000675615.1:c.258T>C	ENSP00000502413.1:p.Gly86=
ENST00000675674.1:n.221T>C
ENST00000675873.1:c.221T>C
ENST00000676173.1:n.302T>C
ENST00000676228.1:c.258T>C	ENSP00000502375.1:p.Gly86=
ENST00000255078.7:c.258T>C	ENSP00000255078.3:p.Gly86=
ENST00000539224.1:c.258T>C	ENSP00000440465.1:p.Gly86=
ENST00000544541.1:c.88T>C	ENSP00000443343.1:p.Ter30Arg
ENST00000545146.1:c.*128T>C	ENSP00000456366.1:n.*128T>C
NM_002180.2:c.258T>C , LRG_250t1:c.258T>C	NP_002171.2:p.Gly86=
XM_005273974.2:c.-754T>C	XP_005274031.1:n.-754T>C
XM_005273976.1:c.258T>C	XP_005274033.1:p.Gly86=
XR_247198.1:n.360T>C
XR_949903.1:n.360T>C
XM_005273976.2:c.258T>C	XP_005274033.1:p.Gly86=
XM_017017669.2:c.-656T>C	XP_016873158.1:n.-656T>C
XM_017017671.2:c.258T>C	XP_016873160.1:p.Gly86=
XR_949903.3:n.356T>C
NM_002180.3:c.258T>C MANE Select	NP_002171.2:p.Gly86=