Canonical Allele Identifier: CA119228
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8026
ClinVar RCV Id: RCV003278655 RCV003555975
dbSNP Id: rs74315513
MyVariant Identifiers: chr22:g.24129390C>T (hg19) chr22:g.23787203C>T (hg38)
PubMed: PMID:17357086
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23787203C>T , CM000684.2:g.23787203C>T GRCh38
NC_000022.10:g.24129390C>T , CM000684.1:g.24129390C>T GRCh37
NC_000022.9:g.22459390C>T NCBI36
NG_009303.1:g.5241C>T , LRG_520:g.5241C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.34C>T ENSP00000263121.8:p.Gln12Ter
ENST00000344921.11:c.34C>T ENSP00000340883.6:p.Gln12Ter
ENST00000407082.4:c.34C>T ENSP00000385226.4:p.Gln12Ter
ENST00000407422.8:c.34C>T ENSP00000383984.3:p.Gln12Ter
ENST00000417137.6:c.34C>T ENSP00000388489.2:p.Gln12Ter
ENST00000491967.2:n.224C>T
ENST00000643421.1:n.2C>T
ENST00000644036.2:c.34C>T MANE Select ENSP00000494049.2:p.Gln12Ter
ENST00000644619.1:c.34C>T ENSP00000494695.1:p.Gln12Ter
ENST00000646421.1:n.226C>T
ENST00000646723.1:n.22C>T
ENST00000647057.1:c.34C>T ENSP00000494757.1:p.Gln12Ter
ENST00000263121.11:c.34C>T ENSP00000263121.7:p.Gln12Ter
ENST00000344921.10:c.34C>T ENSP00000340883.6:p.Gln12Ter
ENST00000407082.3:c.34C>T ENSP00000385226.3:p.Gln12Ter
ENST00000407422.7:c.34C>T ENSP00000383984.3:p.Gln12Ter
ENST00000417137.5:c.34C>T ENSP00000388489.1:p.Gln12Ter
NM_001007468.1:c.34C>T NP_001007469.1:p.Gln12Ter
NM_003073.3:c.34C>T , LRG_520t1:c.34C>T NP_003064.2:p.Gln12Ter
XM_011530345.1:c.34C>T XP_011528647.1:p.Gln12Ter
XM_011530346.1:c.34C>T XP_011528648.1:p.Gln12Ter
NM_001007468.2:c.34C>T NP_001007469.1:p.Gln12Ter
NM_001317946.1:c.34C>T NP_001304875.1:p.Gln12Ter
NM_001362877.1:c.34C>T NP_001349806.1:p.Gln12Ter
NM_003073.4:c.34C>T NP_003064.2:p.Gln12Ter
NM_001007468.3:c.34C>T NP_001007469.1:p.Gln12Ter
NM_001317946.2:c.34C>T NP_001304875.1:p.Gln12Ter
NM_001362877.2:c.34C>T NP_001349806.1:p.Gln12Ter
NM_003073.5:c.34C>T MANE Select NP_003064.2:p.Gln12Ter
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