Canonical Allele Identifier: CA475280863

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704354A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936886A>C , CM000673.2:g.68936886A>C	GRCh38
NC_000011.9:g.68704354A>C , CM000673.1:g.68704354A>C	GRCh37
NC_000011.8:g.68460930A>C	NCBI36
NG_007976.1:g.38036A>C , LRG_250:g.38036A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2406A>C MANE Select	ENSP00000255078.4:p.Pro802=
ENST00000674675.1:c.588-37A>C
ENST00000674878.1:c.548-37A>C
ENST00000675118.1:c.1894A>C
ENST00000675389.1:n.681A>C
ENST00000675615.1:c.2406A>C	ENSP00000502413.1:p.Pro802=
ENST00000675648.1:n.1781A>C
ENST00000675916.1:c.650A>C
ENST00000676173.1:n.3151A>C
ENST00000676182.1:c.837A>C
ENST00000676228.1:c.*1729A>C	ENSP00000502375.1:n.*1729A>C
ENST00000255078.7:c.2406A>C	ENSP00000255078.3:p.Pro802=
ENST00000539064.5:n.2165A>C
ENST00000543739.5:n.1399A>C
NM_002180.2:c.2406A>C , LRG_250t1:c.2406A>C	NP_002171.2:p.Pro802=
XM_005273974.2:c.1395A>C	XP_005274031.1:p.Pro465=
XM_005273975.2:c.1278A>C	XP_005274032.1:p.Pro426=
XM_011544994.1:c.1173A>C	XP_011543296.1:p.Pro391=
XR_949903.1:n.2508A>C
XM_005273975.3:c.1278A>C	XP_005274032.1:p.Pro426=
XM_017017669.2:c.1395A>C	XP_016873158.1:p.Pro465=
XM_017017670.2:c.1395A>C	XP_016873159.1:p.Pro465=
XR_949903.3:n.2504A>C
NM_002180.3:c.2406A>C MANE Select	NP_002171.2:p.Pro802=