Canonical Allele Identifier: CA410934125

Gene: SMARCB1

Linked Data

• gnomAD v4: 22-23793687-A-C
• MyVariant Identifiers: chr22:g.24135874A>C (hg19) ; chr22:g.23793687A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23793687A>C , CM000684.2:g.23793687A>C	GRCh38
NC_000022.10:g.24135874A>C , CM000684.1:g.24135874A>C	GRCh37
NC_000022.9:g.22465874A>C	NCBI36
NG_009303.1:g.11725A>C , LRG_520:g.11725A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.361A>C	ENSP00000263121.8:p.Ser121Arg
ENST00000344921.11:c.334A>C	ENSP00000340883.6:p.Arg112=
ENST00000407082.4:c.334A>C	ENSP00000385226.4:p.Ser112Arg
ENST00000407422.8:c.334A>C	ENSP00000383984.3:p.Arg112=
ENST00000417137.6:c.361A>C	ENSP00000388489.2:p.Arg121=
ENST00000491967.2:n.524A>C
ENST00000643421.1:n.329A>C
ENST00000644036.2:c.361A>C MANE Select	ENSP00000494049.2:p.Arg121=
ENST00000644462.1:c.196A>C	ENSP00000494283.1:p.Arg66=
ENST00000644619.1:c.361A>C	ENSP00000494695.1:p.Arg121=
ENST00000646421.1:n.2217A>C
ENST00000646723.1:n.349A>C
ENST00000646911.1:n.273A>C
ENST00000647057.1:c.93+6425A>C	ENSP00000494757.1:n.93+6425A>C
ENST00000263121.11:c.361A>C	ENSP00000263121.7:p.Arg121=
ENST00000344921.10:c.334A>C	ENSP00000340883.6:p.Arg112=
ENST00000407082.3:c.361A>C	ENSP00000385226.3:p.Ser121Arg
ENST00000407422.7:c.334A>C	ENSP00000383984.3:p.Arg112=
ENST00000417137.5:c.361A>C	ENSP00000388489.1:p.Arg121=
ENST00000491967.1:n.87A>C
ENST00000634926.1:c.213A>C
ENST00000635578.1:c.186A>C
NM_001007468.1:c.334A>C	NP_001007469.1:p.Arg112=
NM_003073.3:c.361A>C , LRG_520t1:c.361A>C	NP_003064.2:p.Arg121=
XM_011530345.1:c.361A>C	XP_011528647.1:p.Arg121=
XM_011530346.1:c.334A>C	XP_011528648.1:p.Arg112=
NM_001007468.2:c.334A>C	NP_001007469.1:p.Arg112=
NM_001317946.1:c.334A>C	NP_001304875.1:p.Arg112=
NM_001362877.1:c.361A>C	NP_001349806.1:p.Arg121=
NM_003073.4:c.361A>C	NP_003064.2:p.Arg121=
NM_001007468.3:c.334A>C	NP_001007469.1:p.Arg112=
NM_001317946.2:c.334A>C	NP_001304875.1:p.Arg112=
NM_001362877.2:c.361A>C	NP_001349806.1:p.Arg121=
NM_003073.5:c.361A>C MANE Select	NP_003064.2:p.Arg121=