Canonical Allele Identifier: CA372789112

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2116038G>T (hg19) ; chr9:g.2116038G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2116038G>T , CM000671.2:g.2116038G>T	GRCh38
NC_000009.11:g.2116038G>T , CM000671.1:g.2116038G>T	GRCh37
NC_000009.10:g.2106038G>T	NCBI36
NG_032162.1:g.105697G>T
NG_032162.2:g.140749G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3313G>T	ENSP00000515861.1:p.Glu1105Ter
ENST00000704352.1:c.1174-45648G>T	ENSP00000515863.1:n.1174-45648G>T
ENST00000704353.1:c.1174-45648G>T	ENSP00000515864.1:n.1174-45648G>T
ENST00000704354.1:c.3657G>T
ENST00000704355.1:c.2037G>T
ENST00000349721.8:c.3673G>T MANE Select	ENSP00000265773.5:p.Glu1225Ter
ENST00000357248.8:c.3673G>T	ENSP00000349788.2:p.Glu1225Ter
ENST00000635739.1:n.2341G>T
ENST00000636157.1:n.1280G>T
ENST00000638139.1:n.707G>T
ENST00000349721.7:c.3673G>T	ENSP00000265773.5:p.Glu1225Ter
ENST00000357248.7:c.3673G>T	ENSP00000349788.2:p.Glu1225Ter
ENST00000382194.6:c.3673G>T	ENSP00000371629.1:p.Glu1225Ter
ENST00000382203.5:c.3673G>T	ENSP00000371638.1:p.Glu1225Ter
ENST00000450198.6:c.3499G>T	ENSP00000392081.2:p.Glu1167Ter
ENST00000634760.1:c.3673G>T	ENSP00000489256.1:p.Glu1225Ter
ENST00000634772.1:c.62-3420G>T
ENST00000634925.1:n.1164G>T
NM_001289396.1:c.3673G>T	NP_001276325.1:p.Glu1225Ter
NM_001289397.1:c.3499G>T	NP_001276326.1:p.Glu1167Ter
NM_003070.4:c.3673G>T	NP_003061.3:p.Glu1225Ter
NM_139045.3:c.3673G>T	NP_620614.2:p.Glu1225Ter
NM_003070.5:c.3673G>T MANE Select	NP_003061.3:p.Glu1225Ter
NM_001289397.2:c.3499G>T	NP_001276326.1:p.Glu1167Ter
NM_139045.4:c.3673G>T	NP_620614.2:p.Glu1225Ter