Canonical Allele Identifier: CA410935386

Gene: SMARCB1

Linked Data

• MyVariant Identifiers: chr22:g.24145480A>T (hg19) ; chr22:g.23803293A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23803293A>T , CM000684.2:g.23803293A>T	GRCh38
NC_000022.10:g.24145480A>T , CM000684.1:g.24145480A>T	GRCh37
NC_000022.9:g.22475480A>T	NCBI36
NG_009303.1:g.21331A>T , LRG_520:g.21331A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263121.12:c.363-2A>T	ENSP00000263121.8:n.363-2A>T
ENST00000344921.11:c.528-2A>T	ENSP00000340883.6:n.528-2A>T
ENST00000407082.4:c.336-2A>T	ENSP00000385226.4:n.336-2A>T
ENST00000407422.8:c.474-2A>T	ENSP00000383984.3:n.474-2A>T
ENST00000417137.6:c.555-2A>T	ENSP00000388489.2:n.555-2A>T
ENST00000642275.1:n.747A>T
ENST00000642727.1:c.667-2A>T	ENSP00000495144.1:n.667-2A>T
ENST00000643421.1:n.469-2A>T
ENST00000644036.2:c.501-2A>T MANE Select	ENSP00000494049.2:n.501-2A>T
ENST00000644462.1:c.1219-2A>T	ENSP00000494283.1:n.1219-2A>T
ENST00000644467.1:n.1293A>T
ENST00000644619.1:c.*568-2A>T	ENSP00000494695.1:n.*568-2A>T
ENST00000646723.1:n.2700A>T
ENST00000646911.1:n.413-2A>T
ENST00000647057.1:c.232-2A>T	ENSP00000494757.1:n.232-2A>T
ENST00000263121.11:c.501-2A>T	ENSP00000263121.7:n.501-2A>T
ENST00000344921.10:c.528-2A>T	ENSP00000340883.6:n.528-2A>T
ENST00000407082.3:c.363-2A>T	ENSP00000385226.3:n.363-2A>T
ENST00000407422.7:c.474-2A>T	ENSP00000383984.3:n.474-2A>T
ENST00000417137.5:c.555-2A>T	ENSP00000388489.1:n.555-2A>T
ENST00000634926.1:c.242-2A>T
ENST00000635578.1:c.215-2A>T
NM_001007468.1:c.474-2A>T	NP_001007469.1:n.474-2A>T
NM_003073.3:c.501-2A>T , LRG_520t1:c.501-2A>T	NP_003064.2:n.501-2A>T
XM_011530345.1:c.555-2A>T	XP_011528647.1:n.555-2A>T
XM_011530346.1:c.528-2A>T	XP_011528648.1:n.528-2A>T
NM_001007468.2:c.474-2A>T	NP_001007469.1:n.474-2A>T
NM_001317946.1:c.528-2A>T	NP_001304875.1:n.528-2A>T
NM_001362877.1:c.555-2A>T	NP_001349806.1:n.555-2A>T
NM_003073.4:c.501-2A>T	NP_003064.2:n.501-2A>T
NM_001007468.3:c.474-2A>T	NP_001007469.1:n.474-2A>T
NM_001317946.2:c.528-2A>T	NP_001304875.1:n.528-2A>T
NM_001362877.2:c.555-2A>T	NP_001349806.1:n.555-2A>T
NM_003073.5:c.501-2A>T MANE Select	NP_003064.2:n.501-2A>T