Canonical Allele Identifier: CA410914039

Gene: SMARCB1

Linked Data

• MyVariant Identifiers: chr22:g.24175881G>C (hg19) ; chr22:g.23833694G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23833694G>C , CM000684.2:g.23833694G>C	GRCh38
NC_000022.10:g.24175881G>C , CM000684.1:g.24175881G>C	GRCh37
NC_000022.9:g.22505881G>C	NCBI36
NG_009303.1:g.51732G>C , LRG_520:g.51732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.971G>C	ENSP00000263121.8:p.Arg324Thr
ENST00000344921.11:c.1136G>C	ENSP00000340883.6:p.Arg379Thr
ENST00000407422.8:c.1082G>C	ENSP00000383984.3:p.Arg361Thr
ENST00000644036.2:c.1109G>C MANE Select	ENSP00000494049.2:p.Arg370Thr
ENST00000644462.1:c.1827G>C	ENSP00000494283.1:n.1827G>C
ENST00000645799.1:n.2431G>C
ENST00000646723.1:n.3455G>C
ENST00000647057.1:c.*603G>C	ENSP00000494757.1:n.*603G>C
ENST00000263121.11:c.1109G>C	ENSP00000263121.7:p.Arg370Thr
ENST00000344921.10:c.1136G>C	ENSP00000340883.6:p.Arg379Thr
ENST00000407082.3:c.971G>C	ENSP00000385226.3:p.Arg324Thr
ENST00000407422.7:c.1082G>C	ENSP00000383984.3:p.Arg361Thr
NM_001007468.1:c.1082G>C	NP_001007469.1:p.Arg361Thr
NM_003073.3:c.1109G>C , LRG_520t1:c.1109G>C	NP_003064.2:p.Arg370Thr
XM_011530345.1:c.1163G>C	XP_011528647.1:p.Arg388Thr
XM_011530346.1:c.1136G>C	XP_011528648.1:p.Arg379Thr
NM_001007468.2:c.1082G>C	NP_001007469.1:p.Arg361Thr
NM_001317946.1:c.1136G>C	NP_001304875.1:p.Arg379Thr
NM_001362877.1:c.1163G>C	NP_001349806.1:p.Arg388Thr
NM_003073.4:c.1109G>C	NP_003064.2:p.Arg370Thr
NM_001007468.3:c.1082G>C	NP_001007469.1:p.Arg361Thr
NM_001317946.2:c.1136G>C	NP_001304875.1:p.Arg379Thr
NM_001362877.2:c.1163G>C	NP_001349806.1:p.Arg388Thr
NM_003073.5:c.1109G>C MANE Select	NP_003064.2:p.Arg370Thr