Canonical Allele Identifier: CA475204316

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703772G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936304G>T , CM000673.2:g.68936304G>T	GRCh38
NC_000011.9:g.68703772G>T , CM000673.1:g.68703772G>T	GRCh37
NC_000011.8:g.68460348G>T	NCBI36
NG_007976.1:g.37454G>T , LRG_250:g.37454G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1824G>T MANE Select	ENSP00000255078.4:p.Val608=
ENST00000674675.1:c.68G>T
ENST00000674878.1:c.68G>T
ENST00000674955.1:c.*541G>T	ENSP00000502463.1:n.*541G>T
ENST00000675118.1:c.1312G>T
ENST00000675389.1:n.99G>T
ENST00000675615.1:c.1824G>T	ENSP00000502413.1:p.Val608=
ENST00000675648.1:n.1199G>T
ENST00000675916.1:c.68G>T
ENST00000676173.1:n.2569G>T
ENST00000676182.1:c.255G>T
ENST00000676228.1:c.*1147G>T	ENSP00000502375.1:n.*1147G>T
ENST00000255078.7:c.1824G>T	ENSP00000255078.3:p.Val608=
ENST00000539064.5:n.1583G>T
ENST00000541229.5:n.519G>T
ENST00000543739.5:n.817G>T
ENST00000545475.1:n.420G>T
NM_002180.2:c.1824G>T , LRG_250t1:c.1824G>T	NP_002171.2:p.Val608=
XM_005273974.2:c.813G>T	XP_005274031.1:p.Val271=
XM_005273975.2:c.696G>T	XP_005274032.1:p.Val232=
XM_011544994.1:c.591G>T	XP_011543296.1:p.Val197=
XR_949903.1:n.1926G>T
XM_005273975.3:c.696G>T	XP_005274032.1:p.Val232=
XM_017017669.2:c.813G>T	XP_016873158.1:p.Val271=
XM_017017670.2:c.813G>T	XP_016873159.1:p.Val271=
XR_949903.3:n.1922G>T
NM_002180.3:c.1824G>T MANE Select	NP_002171.2:p.Val608=