Canonical Allele Identifier: CA475280742

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704219G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936751G>T , CM000673.2:g.68936751G>T	GRCh38
NC_000011.9:g.68704219G>T , CM000673.1:g.68704219G>T	GRCh37
NC_000011.8:g.68460795G>T	NCBI36
NG_007976.1:g.37901G>T , LRG_250:g.37901G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2271G>T MANE Select	ENSP00000255078.4:p.Arg757=
ENST00000674675.1:c.515G>T
ENST00000674878.1:c.515G>T
ENST00000674955.1:c.*988G>T	ENSP00000502463.1:n.*988G>T
ENST00000675118.1:c.1759G>T
ENST00000675389.1:n.546G>T
ENST00000675615.1:c.2271G>T	ENSP00000502413.1:p.Arg757=
ENST00000675648.1:n.1646G>T
ENST00000675916.1:c.515G>T
ENST00000676173.1:n.3016G>T
ENST00000676182.1:c.702G>T
ENST00000676228.1:c.*1594G>T	ENSP00000502375.1:n.*1594G>T
ENST00000255078.7:c.2271G>T	ENSP00000255078.3:p.Arg757=
ENST00000539064.5:n.2030G>T
ENST00000543739.5:n.1264G>T
NM_002180.2:c.2271G>T , LRG_250t1:c.2271G>T	NP_002171.2:p.Arg757=
XM_005273974.2:c.1260G>T	XP_005274031.1:p.Arg420=
XM_005273975.2:c.1143G>T	XP_005274032.1:p.Arg381=
XM_011544994.1:c.1038G>T	XP_011543296.1:p.Arg346=
XR_949903.1:n.2373G>T
XM_005273975.3:c.1143G>T	XP_005274032.1:p.Arg381=
XM_017017669.2:c.1260G>T	XP_016873158.1:p.Arg420=
XM_017017670.2:c.1260G>T	XP_016873159.1:p.Arg420=
XR_949903.3:n.2369G>T
NM_002180.3:c.2271G>T MANE Select	NP_002171.2:p.Arg757=