Canonical Allele Identifier: CA410913578

Gene: SMARCB1

Linked Data

• ClinVar Variation Id: 1784737
• ClinVar RCV Id: RCV002419766
• dbSNP Id: rs2146042519
• MyVariant Identifiers: chr22:g.24175847G>A (hg19) ; chr22:g.23833660G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23833660G>A , CM000684.2:g.23833660G>A	GRCh38
NC_000022.10:g.24175847G>A , CM000684.1:g.24175847G>A	GRCh37
NC_000022.9:g.22505847G>A	NCBI36
NG_009303.1:g.51698G>A , LRG_520:g.51698G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.937G>A	ENSP00000263121.8:p.Ala313Thr
ENST00000344921.11:c.1102G>A	ENSP00000340883.6:p.Ala368Thr
ENST00000407422.8:c.1048G>A	ENSP00000383984.3:p.Ala350Thr
ENST00000644036.2:c.1075G>A MANE Select	ENSP00000494049.2:p.Ala359Thr
ENST00000644462.1:c.1793G>A	ENSP00000494283.1:n.1793G>A
ENST00000645799.1:n.2397G>A
ENST00000646723.1:n.3421G>A
ENST00000647057.1:c.*569G>A	ENSP00000494757.1:n.*569G>A
ENST00000263121.11:c.1075G>A	ENSP00000263121.7:p.Ala359Thr
ENST00000344921.10:c.1102G>A	ENSP00000340883.6:p.Ala368Thr
ENST00000407082.3:c.937G>A	ENSP00000385226.3:p.Ala313Thr
ENST00000407422.7:c.1048G>A	ENSP00000383984.3:p.Ala350Thr
NM_001007468.1:c.1048G>A	NP_001007469.1:p.Ala350Thr
NM_003073.3:c.1075G>A , LRG_520t1:c.1075G>A	NP_003064.2:p.Ala359Thr
XM_011530345.1:c.1129G>A	XP_011528647.1:p.Ala377Thr
XM_011530346.1:c.1102G>A	XP_011528648.1:p.Ala368Thr
NM_001007468.2:c.1048G>A	NP_001007469.1:p.Ala350Thr
NM_001317946.1:c.1102G>A	NP_001304875.1:p.Ala368Thr
NM_001362877.1:c.1129G>A	NP_001349806.1:p.Ala377Thr
NM_003073.4:c.1075G>A	NP_003064.2:p.Ala359Thr
NM_001007468.3:c.1048G>A	NP_001007469.1:p.Ala350Thr
NM_001317946.2:c.1102G>A	NP_001304875.1:p.Ala368Thr
NM_001362877.2:c.1129G>A	NP_001349806.1:p.Ala377Thr
NM_003073.5:c.1075G>A MANE Select	NP_003064.2:p.Ala359Thr