Canonical Allele Identifier: CA381644735

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68685213A>G (hg19) ; chr11:g.68917745A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68917745A>G , CM000673.2:g.68917745A>G	GRCh38
NC_000011.9:g.68685213A>G , CM000673.1:g.68685213A>G	GRCh37
NC_000011.8:g.68441789A>G	NCBI36
NG_007976.1:g.18895A>G , LRG_250:g.18895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.922A>G MANE Select	ENSP00000255078.4:p.Lys308Glu
ENST00000539224.2:c.1051A>G
ENST00000674745.1:c.10A>G	ENSP00000502738.1:p.Lys4Glu
ENST00000674775.1:n.10A>G
ENST00000674955.1:c.922A>G	ENSP00000502463.1:p.Lys308Glu
ENST00000675118.1:c.410A>G
ENST00000675119.1:c.349A>G	ENSP00000501861.1:n.349A>G
ENST00000675305.1:c.242A>G	ENSP00000502365.1:n.242A>G
ENST00000675464.1:c.205A>G	ENSP00000502650.1:p.Lys69Glu
ENST00000675493.1:n.10A>G
ENST00000675615.1:c.922A>G	ENSP00000502413.1:p.Lys308Glu
ENST00000675648.1:n.297A>G
ENST00000675683.1:c.309A>G
ENST00000675684.1:c.10A>G	ENSP00000502192.1:p.Lys4Glu
ENST00000676173.1:n.966A>G
ENST00000676228.1:c.*245A>G	ENSP00000502375.1:n.*245A>G
ENST00000255078.7:c.922A>G	ENSP00000255078.3:p.Lys308Glu
NM_002180.2:c.922A>G , LRG_250t1:c.922A>G	NP_002171.2:p.Lys308Glu
XM_005273974.2:c.-90A>G	XP_005274031.1:n.-90A>G
XM_005273976.1:c.922A>G	XP_005274033.1:p.Lys308Glu
XR_247198.1:n.1024A>G
XR_949903.1:n.1024A>G
XM_005273976.2:c.922A>G	XP_005274033.1:p.Lys308Glu
XM_017017669.2:c.-90A>G	XP_016873158.1:n.-90A>G
XM_017017670.2:c.-90A>G	XP_016873159.1:n.-90A>G
XM_017017671.2:c.922A>G	XP_016873160.1:p.Lys308Glu
XR_949903.3:n.1020A>G
NM_002180.3:c.922A>G MANE Select	NP_002171.2:p.Lys308Glu