Canonical Allele Identifier: CA2339299846

Gene: BBC3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47228572C= , CM000681.2:g.47228572C=	GRCh38
NC_000019.9:g.47731829C= , CM000681.1:g.47731829C=	GRCh37
NC_000019.8:g.52423669C=	NCBI36
NG_031991.1:g.9195G=
NG_031991.2:g.9195G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014417.5:c.-15-126G= MANE Select	NP_055232.1:n.-15-126G=
ENST00000439096.3:c.-15-126G= MANE Select	ENSP00000395862.2:n.-15-126G=
NM_001127240.2:c.89-126G=	NP_001120712.1:n.89-126G=
NM_001127240.3:c.89-126G=	NP_001120712.1:n.89-126G=
NM_001127241.2:c.89-1818G=	NP_001120713.1:n.89-1818G=
NM_001127241.3:c.89-1818G=	NP_001120713.1:n.89-1818G=
NM_001127242.2:c.88+3943G=	NP_001120714.1:n.88+3943G=
NM_001127242.3:c.88+3943G=	NP_001120714.1:n.88+3943G=
NM_014417.4:c.-15-126G=	NP_055232.1:n.-15-126G=
ENST00000300880.11:c.88+3943G=	ENSP00000300880.7:n.88+3943G=
ENST00000341983.8:c.89-1818G=	ENSP00000341155.4:n.89-1818G=
ENST00000439096.2:c.-15-126G=	ENSP00000395862.1:n.-15-126G=
ENST00000449228.5:c.89-126G=	ENSP00000404503.1:n.89-126G=
XM_006723141.2:c.-15-126G=	XP_006723204.1:n.-15-126G=
XM_006723141.3:c.-15-126G=	XP_006723204.1:n.-15-126G=
XM_011526722.1:c.34-126G=	XP_011525024.1:n.34-126G=
XM_011526722.2:c.34-126G=	XP_011525024.1:n.34-126G=
XM_011526723.1:c.12-1818G=	XP_011525025.1:n.12-1818G=