Canonical Allele Identifier: CA2397961468
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23793863C= , CM000684.2:g.23793863C= GRCh38
NC_000022.10:g.24136050C= , CM000684.1:g.24136050C= GRCh37
NC_000022.9:g.22466050C= NCBI36
NG_009303.1:g.11901C= , LRG_520:g.11901C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263121.12:c.362+175C= ENSP00000263121.8:n.362+175C=
ENST00000344921.11:c.335+175C= ENSP00000340883.6:n.335+175C=
ENST00000407082.4:c.335+175C= ENSP00000385226.4:n.335+175C=
ENST00000407422.8:c.335+175C= ENSP00000383984.3:n.335+175C=
ENST00000417137.6:c.362+175C= ENSP00000388489.2:n.362+175C=
ENST00000491967.2:n.525+175C=
ENST00000643421.1:n.330+175C=
ENST00000644036.2:c.362+175C= MANE Select ENSP00000494049.2:n.362+175C=
ENST00000644462.1:c.197+175C= ENSP00000494283.1:n.197+175C=
ENST00000644619.1:c.362+175C= ENSP00000494695.1:n.362+175C=
ENST00000646421.1:n.2218+175C=
ENST00000646723.1:n.350+175C=
ENST00000646911.1:n.274+175C=
ENST00000647057.1:c.93+6601C= ENSP00000494757.1:n.93+6601C=
ENST00000263121.11:c.362+175C= ENSP00000263121.7:n.362+175C=
ENST00000344921.10:c.335+175C= ENSP00000340883.6:n.335+175C=
ENST00000407082.3:c.362+175C= ENSP00000385226.3:n.362+175C=
ENST00000407422.7:c.335+175C= ENSP00000383984.3:n.335+175C=
ENST00000417137.5:c.362+175C= ENSP00000388489.1:n.362+175C=
ENST00000491967.1:n.88+175C=
ENST00000634926.1:c.214+175C=
ENST00000635578.1:c.187+175C=
NM_001007468.1:c.335+175C= NP_001007469.1:n.335+175C=
NM_003073.3:c.362+175C= , LRG_520t1:c.362+175C= NP_003064.2:n.362+175C=
XM_011530345.1:c.362+175C= XP_011528647.1:n.362+175C=
XM_011530346.1:c.335+175C= XP_011528648.1:n.335+175C=
NM_001007468.2:c.335+175C= NP_001007469.1:n.335+175C=
NM_001317946.1:c.335+175C= NP_001304875.1:n.335+175C=
NM_001362877.1:c.362+175C= NP_001349806.1:n.362+175C=
NM_003073.4:c.362+175C= NP_003064.2:n.362+175C=
NM_001007468.3:c.335+175C= NP_001007469.1:n.335+175C=
NM_001317946.2:c.335+175C= NP_001304875.1:n.335+175C=
NM_001362877.2:c.362+175C= NP_001349806.1:n.362+175C=
NM_003073.5:c.362+175C= MANE Select NP_003064.2:n.362+175C=