Canonical Allele Identifier: CA2738005543
Gene: SMARCB1 HGNC NCBI

Linked Data

dbSNP Id: rs2146046063

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834248G>A , CM000684.2:g.23834248G>A GRCh38
NC_000022.10:g.24176435G>A , CM000684.1:g.24176435G>A GRCh37
NC_000022.9:g.22506435G>A NCBI36
NG_009303.1:g.52286G>A , LRG_520:g.52286G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*68G>A ENSP00000263121.8:n.*68G>A
ENST00000344921.11:c.*68G>A ENSP00000340883.6:n.*68G>A
ENST00000407422.8:c.*68G>A ENSP00000383984.3:n.*68G>A
ENST00000644036.2:c.*68G>A MANE Select ENSP00000494049.2:n.*68G>A
ENST00000644462.1:c.1944G>A ENSP00000494283.1:n.1944G>A
ENST00000645799.1:n.2548G>A
ENST00000646723.1:n.3572G>A
ENST00000647057.1:c.*720G>A ENSP00000494757.1:n.*720G>A
ENST00000263121.11:c.*68G>A ENSP00000263121.7:n.*68G>A
ENST00000344921.10:c.*68G>A ENSP00000340883.6:n.*68G>A
ENST00000407422.7:c.*68G>A ENSP00000383984.3:n.*68G>A
NM_001007468.1:c.*68G>A NP_001007469.1:n.*68G>A
NM_003073.3:c.*68G>A , LRG_520t1:c.*68G>A NP_003064.2:n.*68G>A
XM_011530345.1:c.*68G>A XP_011528647.1:n.*68G>A
XM_011530346.1:c.*68G>A XP_011528648.1:n.*68G>A
NM_001007468.2:c.*68G>A NP_001007469.1:n.*68G>A
NM_001317946.1:c.*68G>A NP_001304875.1:n.*68G>A
NM_001362877.1:c.*68G>A NP_001349806.1:n.*68G>A
NM_003073.4:c.*68G>A NP_003064.2:n.*68G>A
NM_001007468.3:c.*68G>A NP_001007469.1:n.*68G>A
NM_001317946.2:c.*68G>A NP_001304875.1:n.*68G>A
NM_001362877.2:c.*68G>A NP_001349806.1:n.*68G>A
NM_003073.5:c.*68G>A MANE Select NP_003064.2:n.*68G>A