Canonical Allele Identifier: CA2397958054
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23787001G= , CM000684.2:g.23787001G= GRCh38
NC_000022.10:g.24129188G= , CM000684.1:g.24129188G= GRCh37
NC_000022.9:g.22459188G= NCBI36
NG_009303.1:g.5039G= , LRG_520:g.5039G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344921.11:c.-169G= ENSP00000340883.6:n.-169G=
ENST00000407422.8:c.-169G= ENSP00000383984.3:n.-169G=
ENST00000491967.2:n.22G=
ENST00000644036.2:c.-169G= MANE Select ENSP00000494049.2:n.-169G=
ENST00000644619.1:c.-169G= ENSP00000494695.1:n.-169G=
ENST00000646421.1:n.24G=
ENST00000647057.1:c.-169G= ENSP00000494757.1:n.-169G=
ENST00000263121.11:c.-169G= ENSP00000263121.7:n.-169G=
ENST00000344921.10:c.-169G= ENSP00000340883.6:n.-169G=
ENST00000407422.7:c.-169G= ENSP00000383984.3:n.-169G=
ENST00000417137.5:c.-169G= ENSP00000388489.1:n.-169G=
NM_001007468.1:c.-169G= NP_001007469.1:n.-169G=
NM_003073.3:c.-169G= , LRG_520t1:c.-169G= NP_003064.2:n.-169G=
XM_011530345.1:c.-169G= XP_011528647.1:n.-169G=
XM_011530346.1:c.-169G= XP_011528648.1:n.-169G=
NM_001007468.2:c.-169G= NP_001007469.1:n.-169G=
NM_001317946.1:c.-169G= NP_001304875.1:n.-169G=
NM_001362877.1:c.-169G= NP_001349806.1:n.-169G=
NM_003073.4:c.-169G= NP_003064.2:n.-169G=
NM_001007468.3:c.-169G= NP_001007469.1:n.-169G=
NM_001317946.2:c.-169G= NP_001304875.1:n.-169G=
NM_001362877.2:c.-169G= NP_001349806.1:n.-169G=
NM_003073.5:c.-169G= MANE Select NP_003064.2:n.-169G=