Canonical Allele Identifier: CA475200839

Gene: IGHMBP2

Linked Data

• COSMIC: COSM4909908
• MyVariant Identifiers: chr11:g.68701272A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933804A>T , CM000673.2:g.68933804A>T	GRCh38
NC_000011.9:g.68701272A>T , CM000673.1:g.68701272A>T	GRCh37
NC_000011.8:g.68457848A>T	NCBI36
NG_007976.1:g.34954A>T , LRG_250:g.34954A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1428A>T MANE Select	ENSP00000255078.4:p.Pro476=
ENST00000674955.1:c.*145A>T	ENSP00000502463.1:n.*145A>T
ENST00000675118.1:c.916A>T
ENST00000675205.1:n.183+323A>T
ENST00000675615.1:c.1428A>T	ENSP00000502413.1:p.Pro476=
ENST00000675648.1:n.803A>T
ENST00000675997.1:n.113-660A>T
ENST00000676173.1:n.2173A>T
ENST00000676228.1:c.*751A>T	ENSP00000502375.1:n.*751A>T
ENST00000255078.7:c.1428A>T	ENSP00000255078.3:p.Pro476=
ENST00000537458.5:n.545A>T
ENST00000539064.5:n.1187A>T
ENST00000541229.5:n.123A>T
ENST00000543739.5:n.545A>T
NM_002180.2:c.1428A>T , LRG_250t1:c.1428A>T	NP_002171.2:p.Pro476=
XM_005273974.2:c.417A>T	XP_005274031.1:p.Pro139=
XM_005273975.2:c.300A>T	XP_005274032.1:p.Pro100=
XM_011544994.1:c.195A>T	XP_011543296.1:p.Pro65=
XR_949903.1:n.1530A>T
XM_005273975.3:c.300A>T	XP_005274032.1:p.Pro100=
XM_017017669.2:c.417A>T	XP_016873158.1:p.Pro139=
XM_017017670.2:c.417A>T	XP_016873159.1:p.Pro139=
XM_017017671.2:c.1428A>T	XP_016873160.1:p.Pro476=
XR_949903.3:n.1526A>T
NM_002180.3:c.1428A>T MANE Select	NP_002171.2:p.Pro476=