Canonical Allele Identifier: CA322592289
Gene: SMARCB1 HGNC NCBI

Linked Data

dbSNP Id: rs898131569

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23787001G>T , CM000684.2:g.23787001G>T GRCh38
NC_000022.10:g.24129188G>T , CM000684.1:g.24129188G>T GRCh37
NC_000022.9:g.22459188G>T NCBI36
NG_009303.1:g.5039G>T , LRG_520:g.5039G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344921.11:c.-169G>T ENSP00000340883.6:n.-169G>T
ENST00000407422.8:c.-169G>T ENSP00000383984.3:n.-169G>T
ENST00000491967.2:n.22G>T
ENST00000644036.2:c.-169G>T MANE Select ENSP00000494049.2:n.-169G>T
ENST00000644619.1:c.-169G>T ENSP00000494695.1:n.-169G>T
ENST00000646421.1:n.24G>T
ENST00000647057.1:c.-169G>T ENSP00000494757.1:n.-169G>T
ENST00000263121.11:c.-169G>T ENSP00000263121.7:n.-169G>T
ENST00000344921.10:c.-169G>T ENSP00000340883.6:n.-169G>T
ENST00000407422.7:c.-169G>T ENSP00000383984.3:n.-169G>T
ENST00000417137.5:c.-169G>T ENSP00000388489.1:n.-169G>T
NM_001007468.1:c.-169G>T NP_001007469.1:n.-169G>T
NM_003073.3:c.-169G>T , LRG_520t1:c.-169G>T NP_003064.2:n.-169G>T
XM_011530345.1:c.-169G>T XP_011528647.1:n.-169G>T
XM_011530346.1:c.-169G>T XP_011528648.1:n.-169G>T
NM_001007468.2:c.-169G>T NP_001007469.1:n.-169G>T
NM_001317946.1:c.-169G>T NP_001304875.1:n.-169G>T
NM_001362877.1:c.-169G>T NP_001349806.1:n.-169G>T
NM_003073.4:c.-169G>T NP_003064.2:n.-169G>T
NM_001007468.3:c.-169G>T NP_001007469.1:n.-169G>T
NM_001317946.2:c.-169G>T NP_001304875.1:n.-169G>T
NM_001362877.2:c.-169G>T NP_001349806.1:n.-169G>T
NM_003073.5:c.-169G>T MANE Select NP_003064.2:n.-169G>T