Canonical Allele Identifier: CA2397981027
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834045C= , CM000684.2:g.23834045C= GRCh38
NC_000022.10:g.24176232C= , CM000684.1:g.24176232C= GRCh37
NC_000022.9:g.22506232C= NCBI36
NG_009303.1:g.52083C= , LRG_520:g.52083C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.981-96C= ENSP00000263121.8:n.981-96C=
ENST00000344921.11:c.1146-96C= ENSP00000340883.6:n.1146-96C=
ENST00000407422.8:c.1092-96C= ENSP00000383984.3:n.1092-96C=
ENST00000644036.2:c.1119-96C= MANE Select ENSP00000494049.2:n.1119-96C=
ENST00000644462.1:c.1837-96C= ENSP00000494283.1:n.1837-96C=
ENST00000645799.1:n.2441-96C=
ENST00000646723.1:n.3465-96C=
ENST00000647057.1:c.*613-96C= ENSP00000494757.1:n.*613-96C=
ENST00000263121.11:c.1119-96C= ENSP00000263121.7:n.1119-96C=
ENST00000344921.10:c.1146-96C= ENSP00000340883.6:n.1146-96C=
ENST00000407082.3:c.981-96C= ENSP00000385226.3:n.981-96C=
ENST00000407422.7:c.1092-96C= ENSP00000383984.3:n.1092-96C=
NM_001007468.1:c.1092-96C= NP_001007469.1:n.1092-96C=
NM_003073.3:c.1119-96C= , LRG_520t1:c.1119-96C= NP_003064.2:n.1119-96C=
XM_011530345.1:c.1173-96C= XP_011528647.1:n.1173-96C=
XM_011530346.1:c.1146-96C= XP_011528648.1:n.1146-96C=
NM_001007468.2:c.1092-96C= NP_001007469.1:n.1092-96C=
NM_001317946.1:c.1146-96C= NP_001304875.1:n.1146-96C=
NM_001362877.1:c.1173-96C= NP_001349806.1:n.1173-96C=
NM_003073.4:c.1119-96C= NP_003064.2:n.1119-96C=
NM_001007468.3:c.1092-96C= NP_001007469.1:n.1092-96C=
NM_001317946.2:c.1146-96C= NP_001304875.1:n.1146-96C=
NM_001362877.2:c.1173-96C= NP_001349806.1:n.1173-96C=
NM_003073.5:c.1119-96C= MANE Select NP_003064.2:n.1119-96C=