Canonical Allele Identifier: CA410913497

Gene: SMARCB1

Linked Data

• dbSNP Id: rs2146042402
• MyVariant Identifiers: chr22:g.24175836C>G (hg19) ; chr22:g.23833649C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23833649C>G , CM000684.2:g.23833649C>G	GRCh38
NC_000022.10:g.24175836C>G , CM000684.1:g.24175836C>G	GRCh37
NC_000022.9:g.22505836C>G	NCBI36
NG_009303.1:g.51687C>G , LRG_520:g.51687C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.926C>G	ENSP00000263121.8:p.Thr309Ser
ENST00000344921.11:c.1091C>G	ENSP00000340883.6:p.Thr364Ser
ENST00000407422.8:c.1037C>G	ENSP00000383984.3:p.Thr346Ser
ENST00000644036.2:c.1064C>G MANE Select	ENSP00000494049.2:p.Thr355Ser
ENST00000644462.1:c.1782C>G	ENSP00000494283.1:n.1782C>G
ENST00000645799.1:n.2386C>G
ENST00000646723.1:n.3410C>G
ENST00000647057.1:c.*558C>G	ENSP00000494757.1:n.*558C>G
ENST00000263121.11:c.1064C>G	ENSP00000263121.7:p.Thr355Ser
ENST00000344921.10:c.1091C>G	ENSP00000340883.6:p.Thr364Ser
ENST00000407082.3:c.926C>G	ENSP00000385226.3:p.Thr309Ser
ENST00000407422.7:c.1037C>G	ENSP00000383984.3:p.Thr346Ser
NM_001007468.1:c.1037C>G	NP_001007469.1:p.Thr346Ser
NM_003073.3:c.1064C>G , LRG_520t1:c.1064C>G	NP_003064.2:p.Thr355Ser
XM_011530345.1:c.1118C>G	XP_011528647.1:p.Thr373Ser
XM_011530346.1:c.1091C>G	XP_011528648.1:p.Thr364Ser
NM_001007468.2:c.1037C>G	NP_001007469.1:p.Thr346Ser
NM_001317946.1:c.1091C>G	NP_001304875.1:p.Thr364Ser
NM_001362877.1:c.1118C>G	NP_001349806.1:p.Thr373Ser
NM_003073.4:c.1064C>G	NP_003064.2:p.Thr355Ser
NM_001007468.3:c.1037C>G	NP_001007469.1:p.Thr346Ser
NM_001317946.2:c.1091C>G	NP_001304875.1:p.Thr364Ser
NM_001362877.2:c.1118C>G	NP_001349806.1:p.Thr373Ser
NM_003073.5:c.1064C>G MANE Select	NP_003064.2:p.Thr355Ser