Canonical Allele Identifier: CA381644580

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68915003-A-G
• MyVariant Identifiers: chr11:g.68682471A>G (hg19) ; chr11:g.68915003A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915003A>G , CM000673.2:g.68915003A>G	GRCh38
NC_000011.9:g.68682471A>G , CM000673.1:g.68682471A>G	GRCh37
NC_000011.8:g.68439047A>G	NCBI36
NG_007976.1:g.16153A>G , LRG_250:g.16153A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.892A>G MANE Select	ENSP00000255078.4:p.Lys298Glu
ENST00000539224.2:c.1021A>G
ENST00000674955.1:c.892A>G	ENSP00000502463.1:p.Lys298Glu
ENST00000675118.1:c.239A>G
ENST00000675119.1:c.181A>G	ENSP00000501861.1:p.Lys61Glu
ENST00000675305.1:c.181A>G	ENSP00000502365.1:p.Lys61Glu
ENST00000675464.1:c.181A>G	ENSP00000502650.1:p.Lys61Glu
ENST00000675615.1:c.892A>G	ENSP00000502413.1:p.Lys298Glu
ENST00000675683.1:c.279A>G
ENST00000676173.1:n.936A>G
ENST00000676228.1:c.*215A>G	ENSP00000502375.1:n.*215A>G
ENST00000676239.1:n.206A>G
ENST00000255078.7:c.892A>G	ENSP00000255078.3:p.Lys298Glu
NM_002180.2:c.892A>G , LRG_250t1:c.892A>G	NP_002171.2:p.Lys298Glu
XM_005273974.2:c.-120A>G	XP_005274031.1:n.-120A>G
XM_005273976.1:c.892A>G	XP_005274033.1:p.Lys298Glu
XR_247198.1:n.994A>G
XR_949903.1:n.994A>G
XM_005273976.2:c.892A>G	XP_005274033.1:p.Lys298Glu
XM_017017669.2:c.-120A>G	XP_016873158.1:n.-120A>G
XM_017017670.2:c.-120A>G	XP_016873159.1:n.-120A>G
XM_017017671.2:c.892A>G	XP_016873160.1:p.Lys298Glu
XR_949903.3:n.990A>G
NM_002180.3:c.892A>G MANE Select	NP_002171.2:p.Lys298Glu