Canonical Allele Identifier: CA372788708

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2115861C>G (hg19) ; chr9:g.2115861C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115861C>G , CM000671.2:g.2115861C>G	GRCh38
NC_000009.11:g.2115861C>G , CM000671.1:g.2115861C>G	GRCh37
NC_000009.10:g.2105861C>G	NCBI36
NG_032162.1:g.105520C>G
NG_032162.2:g.140572C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000704350.1:c.3136C>G	ENSP00000515861.1:p.Gln1046Glu
ENST00000704352.1:c.1174-45825C>G	ENSP00000515863.1:n.1174-45825C>G
ENST00000704353.1:c.1174-45825C>G	ENSP00000515864.1:n.1174-45825C>G
ENST00000704354.1:c.3480C>G
ENST00000704355.1:c.1860C>G
ENST00000349721.8:c.3496C>G MANE Select	ENSP00000265773.5:p.Gln1166Glu
ENST00000357248.8:c.3496C>G	ENSP00000349788.2:p.Gln1166Glu
ENST00000635739.1:n.2164C>G
ENST00000636157.1:n.1103C>G
ENST00000638139.1:n.530C>G
ENST00000349721.7:c.3496C>G	ENSP00000265773.5:p.Gln1166Glu
ENST00000357248.7:c.3496C>G	ENSP00000349788.2:p.Gln1166Glu
ENST00000382194.6:c.3496C>G	ENSP00000371629.1:p.Gln1166Glu
ENST00000382203.5:c.3496C>G	ENSP00000371638.1:p.Gln1166Glu
ENST00000450198.6:c.3322C>G	ENSP00000392081.2:p.Gln1108Glu
ENST00000634760.1:c.3496C>G	ENSP00000489256.1:p.Gln1166Glu
ENST00000634772.1:c.62-3597C>G
ENST00000634925.1:n.987C>G
NM_001289396.1:c.3496C>G	NP_001276325.1:p.Gln1166Glu
NM_001289397.1:c.3322C>G	NP_001276326.1:p.Gln1108Glu
NM_003070.4:c.3496C>G	NP_003061.3:p.Gln1166Glu
NM_139045.3:c.3496C>G	NP_620614.2:p.Gln1166Glu
NM_003070.5:c.3496C>G MANE Select	NP_003061.3:p.Gln1166Glu
NM_001289397.2:c.3322C>G	NP_001276326.1:p.Gln1108Glu
NM_139045.4:c.3496C>G	NP_620614.2:p.Gln1166Glu