Canonical Allele Identifier: CA2655713954
Gene: SMARCB1 HGNC NCBI

Linked Data

dbSNP Id: rs2146045735

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23834210G>A , CM000684.2:g.23834210G>A GRCh38
NC_000022.10:g.24176397G>A , CM000684.1:g.24176397G>A GRCh37
NC_000022.9:g.22506397G>A NCBI36
NG_009303.1:g.52248G>A , LRG_520:g.52248G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.*30G>A ENSP00000263121.8:n.*30G>A
ENST00000344921.11:c.*30G>A ENSP00000340883.6:n.*30G>A
ENST00000407422.8:c.*30G>A ENSP00000383984.3:n.*30G>A
ENST00000644036.2:c.*30G>A MANE Select ENSP00000494049.2:n.*30G>A
ENST00000644462.1:c.1906G>A ENSP00000494283.1:n.1906G>A
ENST00000645799.1:n.2510G>A
ENST00000646723.1:n.3534G>A
ENST00000647057.1:c.*682G>A ENSP00000494757.1:n.*682G>A
ENST00000263121.11:c.*30G>A ENSP00000263121.7:n.*30G>A
ENST00000344921.10:c.*30G>A ENSP00000340883.6:n.*30G>A
ENST00000407422.7:c.*30G>A ENSP00000383984.3:n.*30G>A
NM_001007468.1:c.*30G>A NP_001007469.1:n.*30G>A
NM_003073.3:c.*30G>A , LRG_520t1:c.*30G>A NP_003064.2:n.*30G>A
XM_011530345.1:c.*30G>A XP_011528647.1:n.*30G>A
XM_011530346.1:c.*30G>A XP_011528648.1:n.*30G>A
NM_001007468.2:c.*30G>A NP_001007469.1:n.*30G>A
NM_001317946.1:c.*30G>A NP_001304875.1:n.*30G>A
NM_001362877.1:c.*30G>A NP_001349806.1:n.*30G>A
NM_003073.4:c.*30G>A NP_003064.2:n.*30G>A
NM_001007468.3:c.*30G>A NP_001007469.1:n.*30G>A
NM_001317946.2:c.*30G>A NP_001304875.1:n.*30G>A
NM_001362877.2:c.*30G>A NP_001349806.1:n.*30G>A
NM_003073.5:c.*30G>A MANE Select NP_003064.2:n.*30G>A