Canonical Allele Identifier: CA381653766

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704435T>G (hg19) ; chr11:g.68936967T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936967T>G , CM000673.2:g.68936967T>G	GRCh38
NC_000011.9:g.68704435T>G , CM000673.1:g.68704435T>G	GRCh37
NC_000011.8:g.68461011T>G	NCBI36
NG_007976.1:g.38117T>G , LRG_250:g.38117T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2487T>G MANE Select	ENSP00000255078.4:p.Asp829Glu
ENST00000674675.1:c.632T>G
ENST00000674878.1:c.592T>G
ENST00000675118.1:c.1975T>G
ENST00000675389.1:n.762T>G
ENST00000675615.1:c.2487T>G	ENSP00000502413.1:p.Asp829Glu
ENST00000675648.1:n.1862T>G
ENST00000675916.1:c.731T>G
ENST00000676173.1:n.3232T>G
ENST00000676182.1:c.918T>G
ENST00000676228.1:c.*1810T>G	ENSP00000502375.1:n.*1810T>G
ENST00000255078.7:c.2487T>G	ENSP00000255078.3:p.Asp829Glu
ENST00000539064.5:n.2246T>G
ENST00000543739.5:n.1480T>G
NM_002180.2:c.2487T>G , LRG_250t1:c.2487T>G	NP_002171.2:p.Asp829Glu
XM_005273974.2:c.1476T>G	XP_005274031.1:p.Asp492Glu
XM_005273975.2:c.1359T>G	XP_005274032.1:p.Asp453Glu
XM_011544994.1:c.1254T>G	XP_011543296.1:p.Asp418Glu
XR_949903.1:n.2589T>G
XM_005273975.3:c.1359T>G	XP_005274032.1:p.Asp453Glu
XM_017017669.2:c.1476T>G	XP_016873158.1:p.Asp492Glu
XM_017017670.2:c.1476T>G	XP_016873159.1:p.Asp492Glu
XR_949903.3:n.2585T>G
NM_002180.3:c.2487T>G MANE Select	NP_002171.2:p.Asp829Glu