Canonical Allele Identifier: CA475279551

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704054G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936586G>C , CM000673.2:g.68936586G>C	GRCh38
NC_000011.9:g.68704054G>C , CM000673.1:g.68704054G>C	GRCh37
NC_000011.8:g.68460630G>C	NCBI36
NG_007976.1:g.37736G>C , LRG_250:g.37736G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2106G>C MANE Select	ENSP00000255078.4:p.Leu702=
ENST00000674675.1:c.350G>C
ENST00000674878.1:c.350G>C
ENST00000674955.1:c.*823G>C	ENSP00000502463.1:n.*823G>C
ENST00000675118.1:c.1594G>C
ENST00000675389.1:n.381G>C
ENST00000675615.1:c.2106G>C	ENSP00000502413.1:p.Leu702=
ENST00000675648.1:n.1481G>C
ENST00000675916.1:c.350G>C
ENST00000676173.1:n.2851G>C
ENST00000676182.1:c.537G>C
ENST00000676228.1:c.*1429G>C	ENSP00000502375.1:n.*1429G>C
ENST00000255078.7:c.2106G>C	ENSP00000255078.3:p.Leu702=
ENST00000539064.5:n.1865G>C
ENST00000543739.5:n.1099G>C
NM_002180.2:c.2106G>C , LRG_250t1:c.2106G>C	NP_002171.2:p.Leu702=
XM_005273974.2:c.1095G>C	XP_005274031.1:p.Leu365=
XM_005273975.2:c.978G>C	XP_005274032.1:p.Leu326=
XM_011544994.1:c.873G>C	XP_011543296.1:p.Leu291=
XR_949903.1:n.2208G>C
XM_005273975.3:c.978G>C	XP_005274032.1:p.Leu326=
XM_017017669.2:c.1095G>C	XP_016873158.1:p.Leu365=
XM_017017670.2:c.1095G>C	XP_016873159.1:p.Leu365=
XR_949903.3:n.2204G>C
NM_002180.3:c.2106G>C MANE Select	NP_002171.2:p.Leu702=