Canonical Allele Identifier: CA410913376

Gene: SMARCB1

Linked Data

• ClinVar Variation Id: 850717
• ClinVar RCV Id: RCV001054947 ; RCV002400314
• dbSNP Id: rs2030790017
• MyVariant Identifiers: chr22:g.24175824C>T (hg19) ; chr22:g.23833637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23833637C>T , CM000684.2:g.23833637C>T	GRCh38
NC_000022.10:g.24175824C>T , CM000684.1:g.24175824C>T	GRCh37
NC_000022.9:g.22505824C>T	NCBI36
NG_009303.1:g.51675C>T , LRG_520:g.51675C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.914C>T	ENSP00000263121.8:p.Pro305Leu
ENST00000344921.11:c.1079C>T	ENSP00000340883.6:p.Pro360Leu
ENST00000407422.8:c.1025C>T	ENSP00000383984.3:p.Pro342Leu
ENST00000644036.2:c.1052C>T MANE Select	ENSP00000494049.2:p.Pro351Leu
ENST00000644462.1:c.1770C>T	ENSP00000494283.1:n.1770C>T
ENST00000645799.1:n.2374C>T
ENST00000646723.1:n.3398C>T
ENST00000647057.1:c.*546C>T	ENSP00000494757.1:n.*546C>T
ENST00000263121.11:c.1052C>T	ENSP00000263121.7:p.Pro351Leu
ENST00000344921.10:c.1079C>T	ENSP00000340883.6:p.Pro360Leu
ENST00000407082.3:c.914C>T	ENSP00000385226.3:p.Pro305Leu
ENST00000407422.7:c.1025C>T	ENSP00000383984.3:p.Pro342Leu
NM_001007468.1:c.1025C>T	NP_001007469.1:p.Pro342Leu
NM_003073.3:c.1052C>T , LRG_520t1:c.1052C>T	NP_003064.2:p.Pro351Leu
XM_011530345.1:c.1106C>T	XP_011528647.1:p.Pro369Leu
XM_011530346.1:c.1079C>T	XP_011528648.1:p.Pro360Leu
NM_001007468.2:c.1025C>T	NP_001007469.1:p.Pro342Leu
NM_001317946.1:c.1079C>T	NP_001304875.1:p.Pro360Leu
NM_001362877.1:c.1106C>T	NP_001349806.1:p.Pro369Leu
NM_003073.4:c.1052C>T	NP_003064.2:p.Pro351Leu
NM_001007468.3:c.1025C>T	NP_001007469.1:p.Pro342Leu
NM_001317946.2:c.1079C>T	NP_001304875.1:p.Pro360Leu
NM_001362877.2:c.1106C>T	NP_001349806.1:p.Pro369Leu
NM_003073.5:c.1052C>T MANE Select	NP_003064.2:p.Pro351Leu