Canonical Allele Identifier: CA2397961337
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23793593C= , CM000684.2:g.23793593C= GRCh38
NC_000022.10:g.24135780C= , CM000684.1:g.24135780C= GRCh37
NC_000022.9:g.22465780C= NCBI36
NG_009303.1:g.11631C= , LRG_520:g.11631C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.267C= ENSP00000263121.8:p.Thr89=
ENST00000344921.11:c.240C= ENSP00000340883.6:p.Thr80=
ENST00000407082.4:c.240C= ENSP00000385226.4:p.Thr80=
ENST00000407422.8:c.240C= ENSP00000383984.3:p.Thr80=
ENST00000417137.6:c.267C= ENSP00000388489.2:p.Thr89=
ENST00000491967.2:n.430C=
ENST00000643421.1:n.235C=
ENST00000644036.2:c.267C= MANE Select ENSP00000494049.2:p.Thr89=
ENST00000644462.1:c.102C= ENSP00000494283.1:p.Thr34=
ENST00000644619.1:c.267C= ENSP00000494695.1:p.Thr89=
ENST00000646421.1:n.2123C=
ENST00000646723.1:n.255C=
ENST00000646911.1:n.179C=
ENST00000647057.1:c.93+6331C= ENSP00000494757.1:n.93+6331C=
ENST00000263121.11:c.267C= ENSP00000263121.7:p.Thr89=
ENST00000344921.10:c.240C= ENSP00000340883.6:p.Thr80=
ENST00000407082.3:c.267C= ENSP00000385226.3:p.Thr89=
ENST00000407422.7:c.240C= ENSP00000383984.3:p.Thr80=
ENST00000417137.5:c.267C= ENSP00000388489.1:p.Thr89=
ENST00000634926.1:c.119C=
ENST00000635578.1:c.92C=
NM_001007468.1:c.240C= NP_001007469.1:p.Thr80=
NM_003073.3:c.267C= , LRG_520t1:c.267C= NP_003064.2:p.Thr89=
XM_011530345.1:c.267C= XP_011528647.1:p.Thr89=
XM_011530346.1:c.240C= XP_011528648.1:p.Thr80=
NM_001007468.2:c.240C= NP_001007469.1:p.Thr80=
NM_001317946.1:c.240C= NP_001304875.1:p.Thr80=
NM_001362877.1:c.267C= NP_001349806.1:p.Thr89=
NM_003073.4:c.267C= NP_003064.2:p.Thr89=
NM_001007468.3:c.240C= NP_001007469.1:p.Thr80=
NM_001317946.2:c.240C= NP_001304875.1:p.Thr80=
NM_001362877.2:c.267C= NP_001349806.1:p.Thr89=
NM_003073.5:c.267C= MANE Select NP_003064.2:p.Thr89=