Canonical Allele Identifier: CA2655703737
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23803204C>A , CM000684.2:g.23803204C>A GRCh38
NC_000022.10:g.24145391C>A , CM000684.1:g.24145391C>A GRCh37
NC_000022.9:g.22475391C>A NCBI36
NG_009303.1:g.21242C>A , LRG_520:g.21242C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.363-91C>A ENSP00000263121.8:n.363-91C>A
ENST00000344921.11:c.528-91C>A ENSP00000340883.6:n.528-91C>A
ENST00000407082.4:c.336-91C>A ENSP00000385226.4:n.336-91C>A
ENST00000407422.8:c.474-91C>A ENSP00000383984.3:n.474-91C>A
ENST00000417137.6:c.555-91C>A ENSP00000388489.2:n.555-91C>A
ENST00000642275.1:n.658C>A
ENST00000642727.1:c.667-91C>A ENSP00000495144.1:n.667-91C>A
ENST00000643421.1:n.469-91C>A
ENST00000644036.2:c.501-91C>A MANE Select ENSP00000494049.2:n.501-91C>A
ENST00000644462.1:c.1219-91C>A ENSP00000494283.1:n.1219-91C>A
ENST00000644467.1:n.1204C>A
ENST00000644619.1:c.*568-91C>A ENSP00000494695.1:n.*568-91C>A
ENST00000646723.1:n.2611C>A
ENST00000646911.1:n.413-91C>A
ENST00000647057.1:c.232-91C>A ENSP00000494757.1:n.232-91C>A
ENST00000263121.11:c.501-91C>A ENSP00000263121.7:n.501-91C>A
ENST00000344921.10:c.528-91C>A ENSP00000340883.6:n.528-91C>A
ENST00000407082.3:c.363-91C>A ENSP00000385226.3:n.363-91C>A
ENST00000407422.7:c.474-91C>A ENSP00000383984.3:n.474-91C>A
ENST00000417137.5:c.555-91C>A ENSP00000388489.1:n.555-91C>A
ENST00000634926.1:c.242-91C>A
ENST00000635578.1:c.215-91C>A
NM_001007468.1:c.474-91C>A NP_001007469.1:n.474-91C>A
NM_003073.3:c.501-91C>A , LRG_520t1:c.501-91C>A NP_003064.2:n.501-91C>A
XM_011530345.1:c.555-91C>A XP_011528647.1:n.555-91C>A
XM_011530346.1:c.528-91C>A XP_011528648.1:n.528-91C>A
NM_001007468.2:c.474-91C>A NP_001007469.1:n.474-91C>A
NM_001317946.1:c.528-91C>A NP_001304875.1:n.528-91C>A
NM_001362877.1:c.555-91C>A NP_001349806.1:n.555-91C>A
NM_003073.4:c.501-91C>A NP_003064.2:n.501-91C>A
NM_001007468.3:c.474-91C>A NP_001007469.1:n.474-91C>A
NM_001317946.2:c.528-91C>A NP_001304875.1:n.528-91C>A
NM_001362877.2:c.555-91C>A NP_001349806.1:n.555-91C>A
NM_003073.5:c.501-91C>A MANE Select NP_003064.2:n.501-91C>A