Canonical Allele Identifier: CA475280768

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704267G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936799G>A , CM000673.2:g.68936799G>A	GRCh38
NC_000011.9:g.68704267G>A , CM000673.1:g.68704267G>A	GRCh37
NC_000011.8:g.68460843G>A	NCBI36
NG_007976.1:g.37949G>A , LRG_250:g.37949G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2319G>A MANE Select	ENSP00000255078.4:p.Gly773=
ENST00000674675.1:c.563G>A
ENST00000674878.1:c.547+16G>A
ENST00000674955.1:c.*1036G>A	ENSP00000502463.1:n.*1036G>A
ENST00000675118.1:c.1807G>A
ENST00000675389.1:n.594G>A
ENST00000675615.1:c.2319G>A	ENSP00000502413.1:p.Gly773=
ENST00000675648.1:n.1694G>A
ENST00000675916.1:c.563G>A
ENST00000676173.1:n.3064G>A
ENST00000676182.1:c.750G>A
ENST00000676228.1:c.*1642G>A	ENSP00000502375.1:n.*1642G>A
ENST00000255078.7:c.2319G>A	ENSP00000255078.3:p.Gly773=
ENST00000539064.5:n.2078G>A
ENST00000543739.5:n.1312G>A
NM_002180.2:c.2319G>A , LRG_250t1:c.2319G>A	NP_002171.2:p.Gly773=
XM_005273974.2:c.1308G>A	XP_005274031.1:p.Gly436=
XM_005273975.2:c.1191G>A	XP_005274032.1:p.Gly397=
XM_011544994.1:c.1086G>A	XP_011543296.1:p.Gly362=
XR_949903.1:n.2421G>A
XM_005273975.3:c.1191G>A	XP_005274032.1:p.Gly397=
XM_017017669.2:c.1308G>A	XP_016873158.1:p.Gly436=
XM_017017670.2:c.1308G>A	XP_016873159.1:p.Gly436=
XR_949903.3:n.2417G>A
NM_002180.3:c.2319G>A MANE Select	NP_002171.2:p.Gly773=