Canonical Allele Identifier: CA410914719
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 651993
dbSNP Id: rs1387467529

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834164C>T , CM000684.2:g.23834164C>T GRCh38
NC_000022.10:g.24176351C>T , CM000684.1:g.24176351C>T GRCh37
NC_000022.9:g.22506351C>T NCBI36
NG_009303.1:g.52202C>T , LRG_520:g.52202C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.1004C>T ENSP00000263121.8:p.Thr335Met
ENST00000344921.11:c.1169C>T ENSP00000340883.6:p.Thr390Met
ENST00000407422.8:c.1115C>T ENSP00000383984.3:p.Thr372Met
ENST00000644036.2:c.1142C>T MANE Select ENSP00000494049.2:p.Thr381Met
ENST00000644462.1:c.1860C>T ENSP00000494283.1:n.1860C>T
ENST00000645799.1:n.2464C>T
ENST00000646723.1:n.3488C>T
ENST00000647057.1:c.*636C>T ENSP00000494757.1:n.*636C>T
ENST00000263121.11:c.1142C>T ENSP00000263121.7:p.Thr381Met
ENST00000344921.10:c.1169C>T ENSP00000340883.6:p.Thr390Met
ENST00000407082.3:c.1004C>T ENSP00000385226.3:p.Thr335Met
ENST00000407422.7:c.1115C>T ENSP00000383984.3:p.Thr372Met
NM_001007468.1:c.1115C>T NP_001007469.1:p.Thr372Met
NM_003073.3:c.1142C>T , LRG_520t1:c.1142C>T NP_003064.2:p.Thr381Met
XM_011530345.1:c.1196C>T XP_011528647.1:p.Thr399Met
XM_011530346.1:c.1169C>T XP_011528648.1:p.Thr390Met
NM_001007468.2:c.1115C>T NP_001007469.1:p.Thr372Met
NM_001317946.1:c.1169C>T NP_001304875.1:p.Thr390Met
NM_001362877.1:c.1196C>T NP_001349806.1:p.Thr399Met
NM_003073.4:c.1142C>T NP_003064.2:p.Thr381Met
NM_001007468.3:c.1115C>T NP_001007469.1:p.Thr372Met
NM_001317946.2:c.1169C>T NP_001304875.1:p.Thr390Met
NM_001362877.2:c.1196C>T NP_001349806.1:p.Thr399Met
NM_003073.5:c.1142C>T MANE Select NP_003064.2:p.Thr381Met