Canonical Allele Identifier: CA410930690

Gene: SMARCB1

Linked Data

• MyVariant Identifiers: chr22:g.24129403A>C (hg19) ; chr22:g.23787216A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23787216A>C , CM000684.2:g.23787216A>C	GRCh38
NC_000022.10:g.24129403A>C , CM000684.1:g.24129403A>C	GRCh37
NC_000022.9:g.22459403A>C	NCBI36
NG_009303.1:g.5254A>C , LRG_520:g.5254A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263121.12:c.47A>C	ENSP00000263121.8:p.Lys16Thr
ENST00000344921.11:c.47A>C	ENSP00000340883.6:p.Lys16Thr
ENST00000407082.4:c.47A>C	ENSP00000385226.4:p.Lys16Thr
ENST00000407422.8:c.47A>C	ENSP00000383984.3:p.Lys16Thr
ENST00000417137.6:c.47A>C	ENSP00000388489.2:p.Lys16Thr
ENST00000491967.2:n.237A>C
ENST00000643421.1:n.15A>C
ENST00000644036.2:c.47A>C MANE Select	ENSP00000494049.2:p.Lys16Thr
ENST00000644619.1:c.47A>C	ENSP00000494695.1:p.Lys16Thr
ENST00000646421.1:n.239A>C
ENST00000646723.1:n.35A>C
ENST00000647057.1:c.47A>C	ENSP00000494757.1:p.Lys16Thr
ENST00000263121.11:c.47A>C	ENSP00000263121.7:p.Lys16Thr
ENST00000344921.10:c.47A>C	ENSP00000340883.6:p.Lys16Thr
ENST00000407082.3:c.47A>C	ENSP00000385226.3:p.Lys16Thr
ENST00000407422.7:c.47A>C	ENSP00000383984.3:p.Lys16Thr
ENST00000417137.5:c.47A>C	ENSP00000388489.1:p.Lys16Thr
NM_001007468.1:c.47A>C	NP_001007469.1:p.Lys16Thr
NM_003073.3:c.47A>C , LRG_520t1:c.47A>C	NP_003064.2:p.Lys16Thr
XM_011530345.1:c.47A>C	XP_011528647.1:p.Lys16Thr
XM_011530346.1:c.47A>C	XP_011528648.1:p.Lys16Thr
NM_001007468.2:c.47A>C	NP_001007469.1:p.Lys16Thr
NM_001317946.1:c.47A>C	NP_001304875.1:p.Lys16Thr
NM_001362877.1:c.47A>C	NP_001349806.1:p.Lys16Thr
NM_003073.4:c.47A>C	NP_003064.2:p.Lys16Thr
NM_001007468.3:c.47A>C	NP_001007469.1:p.Lys16Thr
NM_001317946.2:c.47A>C	NP_001304875.1:p.Lys16Thr
NM_001362877.2:c.47A>C	NP_001349806.1:p.Lys16Thr
NM_003073.5:c.47A>C MANE Select	NP_003064.2:p.Lys16Thr