Canonical Allele Identifier: CA475195078

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68685288A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68917820A>C , CM000673.2:g.68917820A>C	GRCh38
NC_000011.9:g.68685288A>C , CM000673.1:g.68685288A>C	GRCh37
NC_000011.8:g.68441864A>C	NCBI36
NG_007976.1:g.18970A>C , LRG_250:g.18970A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.997A>C MANE Select	ENSP00000255078.4:p.Arg333=
ENST00000674745.1:c.85A>C	ENSP00000502738.1:p.Arg29=
ENST00000674775.1:n.85A>C
ENST00000674955.1:c.997A>C	ENSP00000502463.1:p.Arg333=
ENST00000675118.1:c.485A>C
ENST00000675119.1:c.424A>C	ENSP00000501861.1:n.424A>C
ENST00000675305.1:c.317A>C	ENSP00000502365.1:n.317A>C
ENST00000675464.1:c.280A>C	ENSP00000502650.1:p.Arg94=
ENST00000675493.1:n.85A>C
ENST00000675615.1:c.997A>C	ENSP00000502413.1:p.Arg333=
ENST00000675648.1:n.372A>C
ENST00000675683.1:c.384A>C
ENST00000675684.1:c.85A>C	ENSP00000502192.1:p.Arg29=
ENST00000676173.1:n.1041A>C
ENST00000676228.1:c.*320A>C	ENSP00000502375.1:n.*320A>C
ENST00000255078.7:c.997A>C	ENSP00000255078.3:p.Arg333=
NM_002180.2:c.997A>C , LRG_250t1:c.997A>C	NP_002171.2:p.Arg333=
XM_005273974.2:c.-15A>C	XP_005274031.1:n.-15A>C
XM_005273976.1:c.997A>C	XP_005274033.1:p.Arg333=
XR_247198.1:n.1099A>C
XR_949903.1:n.1099A>C
XM_005273976.2:c.997A>C	XP_005274033.1:p.Arg333=
XM_017017669.2:c.-15A>C	XP_016873158.1:n.-15A>C
XM_017017670.2:c.-15A>C	XP_016873159.1:n.-15A>C
XM_017017671.2:c.997A>C	XP_016873160.1:p.Arg333=
XR_949903.3:n.1095A>C
NM_002180.3:c.997A>C MANE Select	NP_002171.2:p.Arg333=