Canonical Allele Identifier: CA475204560

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704495C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937027C>G , CM000673.2:g.68937027C>G	GRCh38
NC_000011.9:g.68704495C>G , CM000673.1:g.68704495C>G	GRCh37
NC_000011.8:g.68461071C>G	NCBI36
NG_007976.1:g.38177C>G , LRG_250:g.38177C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2547C>G MANE Select	ENSP00000255078.4:p.Ala849=
ENST00000674675.1:c.692C>G
ENST00000674878.1:c.652C>G
ENST00000675118.1:c.2035C>G
ENST00000675389.1:n.822C>G
ENST00000675615.1:c.2547C>G	ENSP00000502413.1:p.Ala849=
ENST00000675648.1:n.1922C>G
ENST00000675916.1:c.791C>G
ENST00000676173.1:n.3292C>G
ENST00000676182.1:c.978C>G
ENST00000676228.1:c.*1870C>G	ENSP00000502375.1:n.*1870C>G
ENST00000255078.7:c.2547C>G	ENSP00000255078.3:p.Ala849=
ENST00000539064.5:n.2306C>G
ENST00000543739.5:n.1540C>G
NM_002180.2:c.2547C>G , LRG_250t1:c.2547C>G	NP_002171.2:p.Ala849=
XM_005273974.2:c.1536C>G	XP_005274031.1:p.Ala512=
XM_005273975.2:c.1419C>G	XP_005274032.1:p.Ala473=
XM_011544994.1:c.1314C>G	XP_011543296.1:p.Ala438=
XR_949903.1:n.2649C>G
XM_005273975.3:c.1419C>G	XP_005274032.1:p.Ala473=
XM_017017669.2:c.1536C>G	XP_016873158.1:p.Ala512=
XM_017017670.2:c.1536C>G	XP_016873159.1:p.Ala512=
XR_949903.3:n.2645C>G
NM_002180.3:c.2547C>G MANE Select	NP_002171.2:p.Ala849=