Canonical Allele Identifier: CA6153430

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs767156490
• ExAC: 11:68682477 A / G
• gnomAD v2: 11-68682477-A-G
• gnomAD v4: 11-68915009-A-G
• MyVariant Identifiers: chr11:g.68682477A>G (hg19) ; chr11:g.68915009A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915009A>G , CM000673.2:g.68915009A>G	GRCh38
NC_000011.9:g.68682477A>G , CM000673.1:g.68682477A>G	GRCh37
NC_000011.8:g.68439053A>G	NCBI36
NG_007976.1:g.16159A>G , LRG_250:g.16159A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.898A>G MANE Select	ENSP00000255078.4:p.Ile300Val
ENST00000539224.2:c.1027A>G
ENST00000674955.1:c.898A>G	ENSP00000502463.1:p.Ile300Val
ENST00000675118.1:c.245A>G
ENST00000675119.1:c.187A>G	ENSP00000501861.1:p.Ile63Val
ENST00000675305.1:c.187A>G	ENSP00000502365.1:p.Ile63Val
ENST00000675464.1:c.187A>G	ENSP00000502650.1:p.Ile63Val
ENST00000675615.1:c.898A>G	ENSP00000502413.1:p.Ile300Val
ENST00000675683.1:c.285A>G
ENST00000676173.1:n.942A>G
ENST00000676228.1:c.*221A>G	ENSP00000502375.1:n.*221A>G
ENST00000676239.1:n.212A>G
ENST00000255078.7:c.898A>G	ENSP00000255078.3:p.Ile300Val
NM_002180.2:c.898A>G , LRG_250t1:c.898A>G	NP_002171.2:p.Ile300Val
XM_005273974.2:c.-114A>G	XP_005274031.1:n.-114A>G
XM_005273976.1:c.898A>G	XP_005274033.1:p.Ile300Val
XR_247198.1:n.1000A>G
XR_949903.1:n.1000A>G
XM_005273976.2:c.898A>G	XP_005274033.1:p.Ile300Val
XM_017017669.2:c.-114A>G	XP_016873158.1:n.-114A>G
XM_017017670.2:c.-114A>G	XP_016873159.1:n.-114A>G
XM_017017671.2:c.898A>G	XP_016873160.1:p.Ile300Val
XR_949903.3:n.996A>G
NM_002180.3:c.898A>G MANE Select	NP_002171.2:p.Ile300Val