Canonical Allele Identifier: CA381644890

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68685282A>G (hg19) ; chr11:g.68917814A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68917814A>G , CM000673.2:g.68917814A>G	GRCh38
NC_000011.9:g.68685282A>G , CM000673.1:g.68685282A>G	GRCh37
NC_000011.8:g.68441858A>G	NCBI36
NG_007976.1:g.18964A>G , LRG_250:g.18964A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.991A>G MANE Select	ENSP00000255078.4:p.Lys331Glu
ENST00000674745.1:c.79A>G	ENSP00000502738.1:p.Lys27Glu
ENST00000674775.1:n.79A>G
ENST00000674955.1:c.991A>G	ENSP00000502463.1:p.Lys331Glu
ENST00000675118.1:c.479A>G
ENST00000675119.1:c.418A>G	ENSP00000501861.1:n.418A>G
ENST00000675305.1:c.311A>G	ENSP00000502365.1:n.311A>G
ENST00000675464.1:c.274A>G	ENSP00000502650.1:p.Lys92Glu
ENST00000675493.1:n.79A>G
ENST00000675615.1:c.991A>G	ENSP00000502413.1:p.Lys331Glu
ENST00000675648.1:n.366A>G
ENST00000675683.1:c.378A>G
ENST00000675684.1:c.79A>G	ENSP00000502192.1:p.Lys27Glu
ENST00000676173.1:n.1035A>G
ENST00000676228.1:c.*314A>G	ENSP00000502375.1:n.*314A>G
ENST00000255078.7:c.991A>G	ENSP00000255078.3:p.Lys331Glu
NM_002180.2:c.991A>G , LRG_250t1:c.991A>G	NP_002171.2:p.Lys331Glu
XM_005273974.2:c.-21A>G	XP_005274031.1:n.-21A>G
XM_005273976.1:c.991A>G	XP_005274033.1:p.Lys331Glu
XR_247198.1:n.1093A>G
XR_949903.1:n.1093A>G
XM_005273976.2:c.991A>G	XP_005274033.1:p.Lys331Glu
XM_017017669.2:c.-21A>G	XP_016873158.1:n.-21A>G
XM_017017670.2:c.-21A>G	XP_016873159.1:n.-21A>G
XM_017017671.2:c.991A>G	XP_016873160.1:p.Lys331Glu
XR_949903.3:n.1089A>G
NM_002180.3:c.991A>G MANE Select	NP_002171.2:p.Lys331Glu