Canonical Allele Identifier: CA2397958063

Gene: SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23787005G= , CM000684.2:g.23787005G=	GRCh38
NC_000022.10:g.24129192G= , CM000684.1:g.24129192G=	GRCh37
NC_000022.9:g.22459192G=	NCBI36
NG_009303.1:g.5043G= , LRG_520:g.5043G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344921.11:c.-165G=	ENSP00000340883.6:n.-165G=
ENST00000407422.8:c.-165G=	ENSP00000383984.3:n.-165G=
ENST00000491967.2:n.26G=
ENST00000644036.2:c.-165G= MANE Select	ENSP00000494049.2:n.-165G=
ENST00000644619.1:c.-165G=	ENSP00000494695.1:n.-165G=
ENST00000646421.1:n.28G=
ENST00000647057.1:c.-165G=	ENSP00000494757.1:n.-165G=
ENST00000263121.11:c.-165G=	ENSP00000263121.7:n.-165G=
ENST00000344921.10:c.-165G=	ENSP00000340883.6:n.-165G=
ENST00000407422.7:c.-165G=	ENSP00000383984.3:n.-165G=
ENST00000417137.5:c.-165G=	ENSP00000388489.1:n.-165G=
NM_001007468.1:c.-165G=	NP_001007469.1:n.-165G=
NM_003073.3:c.-165G= , LRG_520t1:c.-165G=	NP_003064.2:n.-165G=
XM_011530345.1:c.-165G=	XP_011528647.1:n.-165G=
XM_011530346.1:c.-165G=	XP_011528648.1:n.-165G=
NM_001007468.2:c.-165G=	NP_001007469.1:n.-165G=
NM_001317946.1:c.-165G=	NP_001304875.1:n.-165G=
NM_001362877.1:c.-165G=	NP_001349806.1:n.-165G=
NM_003073.4:c.-165G=	NP_003064.2:n.-165G=
NM_001007468.3:c.-165G=	NP_001007469.1:n.-165G=
NM_001317946.2:c.-165G=	NP_001304875.1:n.-165G=
NM_001362877.2:c.-165G=	NP_001349806.1:n.-165G=
NM_003073.5:c.-165G= MANE Select	NP_003064.2:n.-165G=