Canonical Allele Identifier: CA381644767

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68685227T>G (hg19) ; chr11:g.68917759T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68917759T>G , CM000673.2:g.68917759T>G	GRCh38
NC_000011.9:g.68685227T>G , CM000673.1:g.68685227T>G	GRCh37
NC_000011.8:g.68441803T>G	NCBI36
NG_007976.1:g.18909T>G , LRG_250:g.18909T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.936T>G MANE Select	ENSP00000255078.4:p.Asp312Glu
ENST00000674745.1:c.24T>G	ENSP00000502738.1:p.Asp8Glu
ENST00000674775.1:n.24T>G
ENST00000674955.1:c.936T>G	ENSP00000502463.1:p.Asp312Glu
ENST00000675118.1:c.424T>G
ENST00000675119.1:c.363T>G	ENSP00000501861.1:n.363T>G
ENST00000675305.1:c.256T>G	ENSP00000502365.1:n.256T>G
ENST00000675464.1:c.219T>G	ENSP00000502650.1:p.Asp73Glu
ENST00000675493.1:n.24T>G
ENST00000675615.1:c.936T>G	ENSP00000502413.1:p.Asp312Glu
ENST00000675648.1:n.311T>G
ENST00000675683.1:c.323T>G
ENST00000675684.1:c.24T>G	ENSP00000502192.1:p.Asp8Glu
ENST00000676173.1:n.980T>G
ENST00000676228.1:c.*259T>G	ENSP00000502375.1:n.*259T>G
ENST00000255078.7:c.936T>G	ENSP00000255078.3:p.Asp312Glu
NM_002180.2:c.936T>G , LRG_250t1:c.936T>G	NP_002171.2:p.Asp312Glu
XM_005273974.2:c.-76T>G	XP_005274031.1:n.-76T>G
XM_005273976.1:c.936T>G	XP_005274033.1:p.Asp312Glu
XR_247198.1:n.1038T>G
XR_949903.1:n.1038T>G
XM_005273976.2:c.936T>G	XP_005274033.1:p.Asp312Glu
XM_017017669.2:c.-76T>G	XP_016873158.1:n.-76T>G
XM_017017670.2:c.-76T>G	XP_016873159.1:n.-76T>G
XM_017017671.2:c.936T>G	XP_016873160.1:p.Asp312Glu
XR_949903.3:n.1034T>G
NM_002180.3:c.936T>G MANE Select	NP_002171.2:p.Asp312Glu