Canonical Allele Identifier: CA513739382

Gene: SMARCB1

Linked Data

• MyVariant Identifiers: chr22:g.24175768T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23833581T>C , CM000684.2:g.23833581T>C	GRCh38
NC_000022.10:g.24175768T>C , CM000684.1:g.24175768T>C	GRCh37
NC_000022.9:g.22505768T>C	NCBI36
NG_009303.1:g.51619T>C , LRG_520:g.51619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.858T>C	ENSP00000263121.8:p.Pro286=
ENST00000344921.11:c.1023T>C	ENSP00000340883.6:p.Pro341=
ENST00000407422.8:c.969T>C	ENSP00000383984.3:p.Pro323=
ENST00000477836.2:n.2147T>C
ENST00000644036.2:c.996T>C MANE Select	ENSP00000494049.2:p.Pro332=
ENST00000644462.1:c.1714T>C	ENSP00000494283.1:n.1714T>C
ENST00000645799.1:n.2318T>C
ENST00000646723.1:n.3342T>C
ENST00000647057.1:c.*490T>C	ENSP00000494757.1:n.*490T>C
ENST00000263121.11:c.996T>C	ENSP00000263121.7:p.Pro332=
ENST00000344921.10:c.1023T>C	ENSP00000340883.6:p.Pro341=
ENST00000407082.3:c.858T>C	ENSP00000385226.3:p.Pro286=
ENST00000407422.7:c.969T>C	ENSP00000383984.3:p.Pro323=
NM_001007468.1:c.969T>C	NP_001007469.1:p.Pro323=
NM_003073.3:c.996T>C , LRG_520t1:c.996T>C	NP_003064.2:p.Pro332=
XM_011530345.1:c.1050T>C	XP_011528647.1:p.Pro350=
XM_011530346.1:c.1023T>C	XP_011528648.1:p.Pro341=
NM_001007468.2:c.969T>C	NP_001007469.1:p.Pro323=
NM_001317946.1:c.1023T>C	NP_001304875.1:p.Pro341=
NM_001362877.1:c.1050T>C	NP_001349806.1:p.Pro350=
NM_003073.4:c.996T>C	NP_003064.2:p.Pro332=
NM_001007468.3:c.969T>C	NP_001007469.1:p.Pro323=
NM_001317946.2:c.1023T>C	NP_001304875.1:p.Pro341=
NM_001362877.2:c.1050T>C	NP_001349806.1:p.Pro350=
NM_003073.5:c.996T>C MANE Select	NP_003064.2:p.Pro332=