Canonical Allele Identifier: CA463852825
Gene: SMARCA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2115995C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2115995C>T , CM000671.2:g.2115995C>T GRCh38
NC_000009.11:g.2115995C>T , CM000671.1:g.2115995C>T GRCh37
NC_000009.10:g.2105995C>T NCBI36
NG_032162.1:g.105654C>T
NG_032162.2:g.140706C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3270C>T ENSP00000515861.1:p.Ser1090=
ENST00000704352.1:c.1174-45691C>T ENSP00000515863.1:n.1174-45691C>T
ENST00000704353.1:c.1174-45691C>T ENSP00000515864.1:n.1174-45691C>T
ENST00000704354.1:c.3614C>T
ENST00000704355.1:c.1994C>T
ENST00000349721.8:c.3630C>T MANE Select ENSP00000265773.5:p.Ser1210=
ENST00000357248.8:c.3630C>T ENSP00000349788.2:p.Ser1210=
ENST00000635739.1:n.2298C>T
ENST00000636157.1:n.1237C>T
ENST00000638139.1:n.664C>T
ENST00000349721.7:c.3630C>T ENSP00000265773.5:p.Ser1210=
ENST00000357248.7:c.3630C>T ENSP00000349788.2:p.Ser1210=
ENST00000382194.6:c.3630C>T ENSP00000371629.1:p.Ser1210=
ENST00000382203.5:c.3630C>T ENSP00000371638.1:p.Ser1210=
ENST00000450198.6:c.3456C>T ENSP00000392081.2:p.Ser1152=
ENST00000634760.1:c.3630C>T ENSP00000489256.1:p.Ser1210=
ENST00000634772.1:c.62-3463C>T
ENST00000634925.1:n.1121C>T
NM_001289396.1:c.3630C>T NP_001276325.1:p.Ser1210=
NM_001289397.1:c.3456C>T NP_001276326.1:p.Ser1152=
NM_003070.4:c.3630C>T NP_003061.3:p.Ser1210=
NM_139045.3:c.3630C>T NP_620614.2:p.Ser1210=
NM_003070.5:c.3630C>T MANE Select NP_003061.3:p.Ser1210=
NM_001289397.2:c.3456C>T NP_001276326.1:p.Ser1152=
NM_139045.4:c.3630C>T NP_620614.2:p.Ser1210=