Canonical Allele Identifier: CA2574904219

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68917710T>A , CM000673.2:g.68917710T>A	GRCh38
NC_000011.9:g.68685178T>A , CM000673.1:g.68685178T>A	GRCh37
NC_000011.8:g.68441754T>A	NCBI36
NG_007976.1:g.18860T>A , LRG_250:g.18860T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.913-26T>A MANE Select	ENSP00000255078.4:n.913-26T>A
ENST00000539224.2:c.1042-26T>A
ENST00000674955.1:c.913-26T>A	ENSP00000502463.1:n.913-26T>A
ENST00000675118.1:c.401-26T>A
ENST00000675119.1:c.340-26T>A	ENSP00000501861.1:n.340-26T>A
ENST00000675305.1:c.233-26T>A	ENSP00000502365.1:n.233-26T>A
ENST00000675464.1:c.196-26T>A	ENSP00000502650.1:n.196-26T>A
ENST00000675615.1:c.913-26T>A	ENSP00000502413.1:n.913-26T>A
ENST00000675648.1:n.288-26T>A
ENST00000675683.1:c.300-26T>A
ENST00000676173.1:n.957-26T>A
ENST00000676228.1:c.*236-26T>A	ENSP00000502375.1:n.*236-26T>A
ENST00000255078.7:c.913-26T>A	ENSP00000255078.3:n.913-26T>A
NM_002180.2:c.913-26T>A , LRG_250t1:c.913-26T>A	NP_002171.2:n.913-26T>A
XM_005273974.2:c.-99-26T>A	XP_005274031.1:n.-99-26T>A
XM_005273976.1:c.913-26T>A	XP_005274033.1:n.913-26T>A
XR_247198.1:n.1015-26T>A
XR_949903.1:n.1015-26T>A
XM_005273976.2:c.913-26T>A	XP_005274033.1:n.913-26T>A
XM_017017669.2:c.-99-26T>A	XP_016873158.1:n.-99-26T>A
XM_017017670.2:c.-99-26T>A	XP_016873159.1:n.-99-26T>A
XM_017017671.2:c.913-26T>A	XP_016873160.1:n.913-26T>A
XR_949903.3:n.1011-26T>A
NM_002180.3:c.913-26T>A MANE Select	NP_002171.2:n.913-26T>A