Canonical Allele Identifier: CA2655697997

Gene: SMARCB1

Linked Data

• gnomAD v4: 22-23786969-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23786969A>G , CM000684.2:g.23786969A>G	GRCh38
NC_000022.10:g.24129156A>G , CM000684.1:g.24129156A>G	GRCh37
NC_000022.9:g.22459156A>G	NCBI36
NG_009303.1:g.5007A>G , LRG_520:g.5007A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344921.11:c.-201A>G	ENSP00000340883.6:n.-201A>G
ENST00000407422.8:c.-201A>G	ENSP00000383984.3:n.-201A>G
ENST00000644036.2:c.-201A>G MANE Select	ENSP00000494049.2:n.-201A>G
ENST00000344921.10:c.-201A>G	ENSP00000340883.6:n.-201A>G
ENST00000417137.5:c.-201A>G	ENSP00000388489.1:n.-201A>G
NM_001007468.1:c.-201A>G	NP_001007469.1:n.-201A>G
NM_003073.3:c.-201A>G , LRG_520t1:c.-201A>G	NP_003064.2:n.-201A>G
NM_001007468.2:c.-201A>G	NP_001007469.1:n.-201A>G
NM_001317946.1:c.-201A>G	NP_001304875.1:n.-201A>G
NM_001362877.1:c.-201A>G	NP_001349806.1:n.-201A>G
NM_003073.4:c.-201A>G	NP_003064.2:n.-201A>G
NM_001007468.3:c.-201A>G	NP_001007469.1:n.-201A>G
NM_001317946.2:c.-201A>G	NP_001304875.1:n.-201A>G
NM_001362877.2:c.-201A>G	NP_001349806.1:n.-201A>G
NM_003073.5:c.-201A>G MANE Select	NP_003064.2:n.-201A>G