Canonical Allele Identifier: CA2581030806

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914852C= , CM000673.2:g.68914852C=	GRCh38
NC_000011.9:g.68682320C= , CM000673.1:g.68682320C=	GRCh37
NC_000011.8:g.68438896C=	NCBI36
NG_007976.1:g.16002C= , LRG_250:g.16002C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.741C= MANE Select	ENSP00000255078.4:p.Ala247=
ENST00000539224.2:c.870C=
ENST00000674955.1:c.741C=	ENSP00000502463.1:p.Ala247=
ENST00000675118.1:c.88C=
ENST00000675119.1:c.30C=	ENSP00000501861.1:p.Ala10=
ENST00000675305.1:c.30C=	ENSP00000502365.1:p.Ala10=
ENST00000675464.1:c.30C=	ENSP00000502650.1:p.Ala10=
ENST00000675615.1:c.741C=	ENSP00000502413.1:p.Ala247=
ENST00000675683.1:c.128C=
ENST00000676173.1:n.785C=
ENST00000676228.1:c.*64C=	ENSP00000502375.1:n.*64C=
ENST00000676239.1:n.55C=
ENST00000255078.7:c.741C=	ENSP00000255078.3:p.Ala247=
ENST00000539224.1:c.*64C=	ENSP00000440465.1:n.*64C=
NM_002180.2:c.741C= , LRG_250t1:c.741C=	NP_002171.2:p.Ala247=
XM_005273974.2:c.-271C=	XP_005274031.1:n.-271C=
XM_005273976.1:c.741C=	XP_005274033.1:p.Ala247=
XR_247198.1:n.843C=
XR_949903.1:n.843C=
XM_005273976.2:c.741C=	XP_005274033.1:p.Ala247=
XM_017017669.2:c.-271C=	XP_016873158.1:n.-271C=
XM_017017670.2:c.-271C=	XP_016873159.1:n.-271C=
XM_017017671.2:c.741C=	XP_016873160.1:p.Ala247=
XR_949903.3:n.839C=
NM_002180.3:c.741C= MANE Select	NP_002171.2:p.Ala247=