Canonical Allele Identifier: CA475280811

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704309G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936841G>T , CM000673.2:g.68936841G>T	GRCh38
NC_000011.9:g.68704309G>T , CM000673.1:g.68704309G>T	GRCh37
NC_000011.8:g.68460885G>T	NCBI36
NG_007976.1:g.37991G>T , LRG_250:g.37991G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2361G>T MANE Select	ENSP00000255078.4:p.Pro787=
ENST00000674675.1:c.587+18G>T
ENST00000674878.1:c.547+58G>T
ENST00000674955.1:c.*1078G>T	ENSP00000502463.1:n.*1078G>T
ENST00000675118.1:c.1849G>T
ENST00000675389.1:n.636G>T
ENST00000675615.1:c.2361G>T	ENSP00000502413.1:p.Pro787=
ENST00000675648.1:n.1736G>T
ENST00000675916.1:c.605G>T
ENST00000676173.1:n.3106G>T
ENST00000676182.1:c.792G>T
ENST00000676228.1:c.*1684G>T	ENSP00000502375.1:n.*1684G>T
ENST00000255078.7:c.2361G>T	ENSP00000255078.3:p.Pro787=
ENST00000539064.5:n.2120G>T
ENST00000543739.5:n.1354G>T
NM_002180.2:c.2361G>T , LRG_250t1:c.2361G>T	NP_002171.2:p.Pro787=
XM_005273974.2:c.1350G>T	XP_005274031.1:p.Pro450=
XM_005273975.2:c.1233G>T	XP_005274032.1:p.Pro411=
XM_011544994.1:c.1128G>T	XP_011543296.1:p.Pro376=
XR_949903.1:n.2463G>T
XM_005273975.3:c.1233G>T	XP_005274032.1:p.Pro411=
XM_017017669.2:c.1350G>T	XP_016873158.1:p.Pro450=
XM_017017670.2:c.1350G>T	XP_016873159.1:p.Pro450=
XR_949903.3:n.2459G>T
NM_002180.3:c.2361G>T MANE Select	NP_002171.2:p.Pro787=