Canonical Allele Identifier: CA1827951812
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2115964A= , CM000671.2:g.2115964A= GRCh38
NC_000009.11:g.2115964A= , CM000671.1:g.2115964A= GRCh37
NC_000009.10:g.2105964A= NCBI36
NG_032162.1:g.105623A=
NG_032162.2:g.140675A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3239A= ENSP00000515861.1:p.Gln1080=
ENST00000704352.1:c.1174-45722A= ENSP00000515863.1:n.1174-45722A=
ENST00000704353.1:c.1174-45722A= ENSP00000515864.1:n.1174-45722A=
ENST00000704354.1:c.3583A=
ENST00000704355.1:c.1963A=
ENST00000349721.8:c.3599A= MANE Select ENSP00000265773.5:p.Gln1200=
ENST00000357248.8:c.3599A= ENSP00000349788.2:p.Gln1200=
ENST00000635739.1:n.2267A=
ENST00000636157.1:n.1206A=
ENST00000638139.1:n.633A=
ENST00000349721.7:c.3599A= ENSP00000265773.5:p.Gln1200=
ENST00000357248.7:c.3599A= ENSP00000349788.2:p.Gln1200=
ENST00000382194.6:c.3599A= ENSP00000371629.1:p.Gln1200=
ENST00000382203.5:c.3599A= ENSP00000371638.1:p.Gln1200=
ENST00000450198.6:c.3425A= ENSP00000392081.2:p.Gln1142=
ENST00000634760.1:c.3599A= ENSP00000489256.1:p.Gln1200=
ENST00000634772.1:c.62-3494A=
ENST00000634925.1:n.1090A=
NM_001289396.1:c.3599A= NP_001276325.1:p.Gln1200=
NM_001289397.1:c.3425A= NP_001276326.1:p.Gln1142=
NM_003070.4:c.3599A= NP_003061.3:p.Gln1200=
NM_139045.3:c.3599A= NP_620614.2:p.Gln1200=
NM_003070.5:c.3599A= MANE Select NP_003061.3:p.Gln1200=
NM_001289397.2:c.3425A= NP_001276326.1:p.Gln1142=
NM_139045.4:c.3599A= NP_620614.2:p.Gln1200=