Canonical Allele Identifier: CA381642417

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68906164G>A , CM000673.2:g.68906164G>A	GRCh38
NC_000011.9:g.68673632G>A , CM000673.1:g.68673632G>A	GRCh37
NC_000011.8:g.68430208G>A	NCBI36
NG_007976.1:g.7314G>A , LRG_250:g.7314G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002180.3:c.182G>A MANE Select	NP_002171.2:p.Gly61Glu
ENST00000255078.8:c.182G>A MANE Select	ENSP00000255078.4:p.Gly61Glu
NM_002180.2:c.182G>A , LRG_250t1:c.182G>A	NP_002171.2:p.Gly61Glu
ENST00000255078.7:c.182G>A	ENSP00000255078.3:p.Gly61Glu
ENST00000539224.1:c.182G>A	ENSP00000440465.1:p.Gly61Glu
ENST00000539224.2:c.145G>A
ENST00000544541.1:c.87-1981G>A	ENSP00000443343.1:n.87-1981G>A
ENST00000545146.1:c.182G>A	ENSP00000456366.1:p.Gly61Glu
ENST00000674583.1:c.145G>A
ENST00000674597.1:c.67+29G>A
ENST00000674729.1:n.125G>A
ENST00000674955.1:c.182G>A	ENSP00000502463.1:p.Gly61Glu
ENST00000675142.1:n.145G>A
ENST00000675469.1:c.96G>A
ENST00000675615.1:c.182G>A	ENSP00000502413.1:p.Gly61Glu
ENST00000675674.1:n.145G>A
ENST00000675800.1:n.127G>A
ENST00000675873.1:c.145G>A
ENST00000676173.1:n.222G>A
ENST00000676228.1:c.182G>A	ENSP00000502375.1:p.Gly61Glu
XM_005273974.2:c.-834G>A	XP_005274031.1:n.-834G>A
XM_005273976.1:c.182G>A	XP_005274033.1:p.Gly61Glu
XM_005273976.2:c.182G>A	XP_005274033.1:p.Gly61Glu
XM_017017669.2:c.-732G>A	XP_016873158.1:n.-732G>A
XM_017017671.2:c.182G>A	XP_016873160.1:p.Gly61Glu
XR_247198.1:n.284G>A
XR_949903.1:n.284G>A
XR_949903.3:n.280G>A