Canonical Allele Identifier: CA513769864

Gene: SMARCB1

Linked Data

• dbSNP Id: rs746745700
• MyVariant Identifiers: chr22:g.24135784T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23793597T>C , CM000684.2:g.23793597T>C	GRCh38
NC_000022.10:g.24135784T>C , CM000684.1:g.24135784T>C	GRCh37
NC_000022.9:g.22465784T>C	NCBI36
NG_009303.1:g.11635T>C , LRG_520:g.11635T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263121.12:c.271T>C	ENSP00000263121.8:p.Leu91=
ENST00000344921.11:c.244T>C	ENSP00000340883.6:p.Leu82=
ENST00000407082.4:c.244T>C	ENSP00000385226.4:p.Leu82=
ENST00000407422.8:c.244T>C	ENSP00000383984.3:p.Leu82=
ENST00000417137.6:c.271T>C	ENSP00000388489.2:p.Leu91=
ENST00000491967.2:n.434T>C
ENST00000643421.1:n.239T>C
ENST00000644036.2:c.271T>C MANE Select	ENSP00000494049.2:p.Leu91=
ENST00000644462.1:c.106T>C	ENSP00000494283.1:p.Leu36=
ENST00000644619.1:c.271T>C	ENSP00000494695.1:p.Leu91=
ENST00000646421.1:n.2127T>C
ENST00000646723.1:n.259T>C
ENST00000646911.1:n.183T>C
ENST00000647057.1:c.93+6335T>C	ENSP00000494757.1:n.93+6335T>C
ENST00000263121.11:c.271T>C	ENSP00000263121.7:p.Leu91=
ENST00000344921.10:c.244T>C	ENSP00000340883.6:p.Leu82=
ENST00000407082.3:c.271T>C	ENSP00000385226.3:p.Leu91=
ENST00000407422.7:c.244T>C	ENSP00000383984.3:p.Leu82=
ENST00000417137.5:c.271T>C	ENSP00000388489.1:p.Leu91=
ENST00000634926.1:c.123T>C
ENST00000635578.1:c.96T>C
NM_001007468.1:c.244T>C	NP_001007469.1:p.Leu82=
NM_003073.3:c.271T>C , LRG_520t1:c.271T>C	NP_003064.2:p.Leu91=
XM_011530345.1:c.271T>C	XP_011528647.1:p.Leu91=
XM_011530346.1:c.244T>C	XP_011528648.1:p.Leu82=
NM_001007468.2:c.244T>C	NP_001007469.1:p.Leu82=
NM_001317946.1:c.244T>C	NP_001304875.1:p.Leu82=
NM_001362877.1:c.271T>C	NP_001349806.1:p.Leu91=
NM_003073.4:c.271T>C	NP_003064.2:p.Leu91=
NM_001007468.3:c.244T>C	NP_001007469.1:p.Leu82=
NM_001317946.2:c.244T>C	NP_001304875.1:p.Leu82=
NM_001362877.2:c.271T>C	NP_001349806.1:p.Leu91=
NM_003073.5:c.271T>C MANE Select	NP_003064.2:p.Leu91=