Canonical Allele Identifier: CA410930725
Gene: SMARCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23787221C>A , CM000684.2:g.23787221C>A GRCh38
NC_000022.10:g.24129408C>A , CM000684.1:g.24129408C>A GRCh37
NC_000022.9:g.22459408C>A NCBI36
NG_009303.1:g.5259C>A , LRG_520:g.5259C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.52C>A ENSP00000263121.8:p.Gln18Lys
ENST00000344921.11:c.52C>A ENSP00000340883.6:p.Gln18Lys
ENST00000407082.4:c.52C>A ENSP00000385226.4:p.Gln18Lys
ENST00000407422.8:c.52C>A ENSP00000383984.3:p.Gln18Lys
ENST00000417137.6:c.52C>A ENSP00000388489.2:p.Gln18Lys
ENST00000491967.2:n.242C>A
ENST00000643421.1:n.20C>A
ENST00000644036.2:c.52C>A MANE Select ENSP00000494049.2:p.Gln18Lys
ENST00000644619.1:c.52C>A ENSP00000494695.1:p.Gln18Lys
ENST00000646421.1:n.244C>A
ENST00000646723.1:n.40C>A
ENST00000647057.1:c.52C>A ENSP00000494757.1:p.Gln18Lys
ENST00000263121.11:c.52C>A ENSP00000263121.7:p.Gln18Lys
ENST00000344921.10:c.52C>A ENSP00000340883.6:p.Gln18Lys
ENST00000407082.3:c.52C>A ENSP00000385226.3:p.Gln18Lys
ENST00000407422.7:c.52C>A ENSP00000383984.3:p.Gln18Lys
ENST00000417137.5:c.52C>A ENSP00000388489.1:p.Gln18Lys
NM_001007468.1:c.52C>A NP_001007469.1:p.Gln18Lys
NM_003073.3:c.52C>A , LRG_520t1:c.52C>A NP_003064.2:p.Gln18Lys
XM_011530345.1:c.52C>A XP_011528647.1:p.Gln18Lys
XM_011530346.1:c.52C>A XP_011528648.1:p.Gln18Lys
NM_001007468.2:c.52C>A NP_001007469.1:p.Gln18Lys
NM_001317946.1:c.52C>A NP_001304875.1:p.Gln18Lys
NM_001362877.1:c.52C>A NP_001349806.1:p.Gln18Lys
NM_003073.4:c.52C>A NP_003064.2:p.Gln18Lys
NM_001007468.3:c.52C>A NP_001007469.1:p.Gln18Lys
NM_001317946.2:c.52C>A NP_001304875.1:p.Gln18Lys
NM_001362877.2:c.52C>A NP_001349806.1:p.Gln18Lys
NM_003073.5:c.52C>A MANE Select NP_003064.2:p.Gln18Lys