Canonical Allele Identifier: CA2655714050
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834233T>C , CM000684.2:g.23834233T>C GRCh38
NC_000022.10:g.24176420T>C , CM000684.1:g.24176420T>C GRCh37
NC_000022.9:g.22506420T>C NCBI36
NG_009303.1:g.52271T>C , LRG_520:g.52271T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*53T>C ENSP00000263121.8:n.*53T>C
ENST00000344921.11:c.*53T>C ENSP00000340883.6:n.*53T>C
ENST00000407422.8:c.*53T>C ENSP00000383984.3:n.*53T>C
ENST00000644036.2:c.*53T>C MANE Select ENSP00000494049.2:n.*53T>C
ENST00000644462.1:c.1929T>C ENSP00000494283.1:n.1929T>C
ENST00000645799.1:n.2533T>C
ENST00000646723.1:n.3557T>C
ENST00000647057.1:c.*705T>C ENSP00000494757.1:n.*705T>C
ENST00000263121.11:c.*53T>C ENSP00000263121.7:n.*53T>C
ENST00000344921.10:c.*53T>C ENSP00000340883.6:n.*53T>C
ENST00000407422.7:c.*53T>C ENSP00000383984.3:n.*53T>C
NM_001007468.1:c.*53T>C NP_001007469.1:n.*53T>C
NM_003073.3:c.*53T>C , LRG_520t1:c.*53T>C NP_003064.2:n.*53T>C
XM_011530345.1:c.*53T>C XP_011528647.1:n.*53T>C
XM_011530346.1:c.*53T>C XP_011528648.1:n.*53T>C
NM_001007468.2:c.*53T>C NP_001007469.1:n.*53T>C
NM_001317946.1:c.*53T>C NP_001304875.1:n.*53T>C
NM_001362877.1:c.*53T>C NP_001349806.1:n.*53T>C
NM_003073.4:c.*53T>C NP_003064.2:n.*53T>C
NM_001007468.3:c.*53T>C NP_001007469.1:n.*53T>C
NM_001317946.2:c.*53T>C NP_001304875.1:n.*53T>C
NM_001362877.2:c.*53T>C NP_001349806.1:n.*53T>C
NM_003073.5:c.*53T>C MANE Select NP_003064.2:n.*53T>C