Canonical Allele Identifier: CA475279277

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704012A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936544A>T , CM000673.2:g.68936544A>T	GRCh38
NC_000011.9:g.68704012A>T , CM000673.1:g.68704012A>T	GRCh37
NC_000011.8:g.68460588A>T	NCBI36
NG_007976.1:g.37694A>T , LRG_250:g.37694A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2064A>T MANE Select	ENSP00000255078.4:p.Ala688=
ENST00000674675.1:c.308A>T
ENST00000674878.1:c.308A>T
ENST00000674955.1:c.*781A>T	ENSP00000502463.1:n.*781A>T
ENST00000675118.1:c.1552A>T
ENST00000675389.1:n.339A>T
ENST00000675615.1:c.2064A>T	ENSP00000502413.1:p.Ala688=
ENST00000675648.1:n.1439A>T
ENST00000675916.1:c.308A>T
ENST00000676173.1:n.2809A>T
ENST00000676182.1:c.495A>T
ENST00000676228.1:c.*1387A>T	ENSP00000502375.1:n.*1387A>T
ENST00000255078.7:c.2064A>T	ENSP00000255078.3:p.Ala688=
ENST00000539064.5:n.1823A>T
ENST00000543739.5:n.1057A>T
NM_002180.2:c.2064A>T , LRG_250t1:c.2064A>T	NP_002171.2:p.Ala688=
XM_005273974.2:c.1053A>T	XP_005274031.1:p.Ala351=
XM_005273975.2:c.936A>T	XP_005274032.1:p.Ala312=
XM_011544994.1:c.831A>T	XP_011543296.1:p.Ala277=
XR_949903.1:n.2166A>T
XM_005273975.3:c.936A>T	XP_005274032.1:p.Ala312=
XM_017017669.2:c.1053A>T	XP_016873158.1:p.Ala351=
XM_017017670.2:c.1053A>T	XP_016873159.1:p.Ala351=
XR_949903.3:n.2162A>T
NM_002180.3:c.2064A>T MANE Select	NP_002171.2:p.Ala688=