Canonical Allele Identifier: CA16616285

Gene: SMARCB1

Linked Data

• ClinVar Variation Id: 410706
• ClinVar RCV Id: RCV000490024 ; RCV000785603 ; RCV002402285
• dbSNP Id: rs779769475
• MyVariant Identifiers: chr22:g.24134007G>T (hg19) ; chr22:g.23791820G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23791820G>T , CM000684.2:g.23791820G>T	GRCh38
NC_000022.10:g.24134007G>T , CM000684.1:g.24134007G>T	GRCh37
NC_000022.9:g.22464007G>T	NCBI36
NG_009303.1:g.9858G>T , LRG_520:g.9858G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.158G>T	ENSP00000263121.8:p.Arg53Leu
ENST00000344921.11:c.158G>T	ENSP00000340883.6:p.Arg53Leu
ENST00000407082.4:c.158G>T	ENSP00000385226.4:p.Arg53Leu
ENST00000407422.8:c.158G>T	ENSP00000383984.3:p.Arg53Leu
ENST00000417137.6:c.158G>T	ENSP00000388489.2:p.Arg53Leu
ENST00000491967.2:n.348G>T
ENST00000643421.1:n.126G>T
ENST00000644036.2:c.158G>T MANE Select	ENSP00000494049.2:p.Arg53Leu
ENST00000644462.1:c.20G>T	ENSP00000494283.1:p.Arg7Leu
ENST00000644619.1:c.158G>T	ENSP00000494695.1:p.Arg53Leu
ENST00000646421.1:n.350G>T
ENST00000646723.1:n.146G>T
ENST00000646911.1:n.70G>T
ENST00000647057.1:c.93+4558G>T	ENSP00000494757.1:n.93+4558G>T
ENST00000263121.11:c.158G>T	ENSP00000263121.7:p.Arg53Leu
ENST00000344921.10:c.158G>T	ENSP00000340883.6:p.Arg53Leu
ENST00000407082.3:c.158G>T	ENSP00000385226.3:p.Arg53Leu
ENST00000407422.7:c.158G>T	ENSP00000383984.3:p.Arg53Leu
ENST00000417137.5:c.158G>T	ENSP00000388489.1:p.Arg53Leu
ENST00000634926.1:c.10G>T
ENST00000635578.1:c.10G>T
NM_001007468.1:c.158G>T	NP_001007469.1:p.Arg53Leu
NM_003073.3:c.158G>T , LRG_520t1:c.158G>T	NP_003064.2:p.Arg53Leu
XM_011530345.1:c.158G>T	XP_011528647.1:p.Arg53Leu
XM_011530346.1:c.158G>T	XP_011528648.1:p.Arg53Leu
NM_001007468.2:c.158G>T	NP_001007469.1:p.Arg53Leu
NM_001317946.1:c.158G>T	NP_001304875.1:p.Arg53Leu
NM_001362877.1:c.158G>T	NP_001349806.1:p.Arg53Leu
NM_003073.4:c.158G>T	NP_003064.2:p.Arg53Leu
NM_001007468.3:c.158G>T	NP_001007469.1:p.Arg53Leu
NM_001317946.2:c.158G>T	NP_001304875.1:p.Arg53Leu
NM_001362877.2:c.158G>T	NP_001349806.1:p.Arg53Leu
NM_003073.5:c.158G>T MANE Select	NP_003064.2:p.Arg53Leu