Canonical Allele Identifier: CA372788740
Gene: SMARCA2 HGNC NCBI

Linked Data

gnomAD v4: 9-2115874-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2115874G>A , CM000671.2:g.2115874G>A GRCh38
NC_000009.11:g.2115874G>A , CM000671.1:g.2115874G>A GRCh37
NC_000009.10:g.2105874G>A NCBI36
NG_032162.1:g.105533G>A
NG_032162.2:g.140585G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3149G>A ENSP00000515861.1:p.Arg1050Gln
ENST00000704352.1:c.1174-45812G>A ENSP00000515863.1:n.1174-45812G>A
ENST00000704353.1:c.1174-45812G>A ENSP00000515864.1:n.1174-45812G>A
ENST00000704354.1:c.3493G>A
ENST00000704355.1:c.1873G>A
ENST00000349721.8:c.3509G>A MANE Select ENSP00000265773.5:p.Arg1170Gln
ENST00000357248.8:c.3509G>A ENSP00000349788.2:p.Arg1170Gln
ENST00000635739.1:n.2177G>A
ENST00000636157.1:n.1116G>A
ENST00000638139.1:n.543G>A
ENST00000349721.7:c.3509G>A ENSP00000265773.5:p.Arg1170Gln
ENST00000357248.7:c.3509G>A ENSP00000349788.2:p.Arg1170Gln
ENST00000382194.6:c.3509G>A ENSP00000371629.1:p.Arg1170Gln
ENST00000382203.5:c.3509G>A ENSP00000371638.1:p.Arg1170Gln
ENST00000450198.6:c.3335G>A ENSP00000392081.2:p.Arg1112Gln
ENST00000634760.1:c.3509G>A ENSP00000489256.1:p.Arg1170Gln
ENST00000634772.1:c.62-3584G>A
ENST00000634925.1:n.1000G>A
NM_001289396.1:c.3509G>A NP_001276325.1:p.Arg1170Gln
NM_001289397.1:c.3335G>A NP_001276326.1:p.Arg1112Gln
NM_003070.4:c.3509G>A NP_003061.3:p.Arg1170Gln
NM_139045.3:c.3509G>A NP_620614.2:p.Arg1170Gln
NM_003070.5:c.3509G>A MANE Select NP_003061.3:p.Arg1170Gln
NM_001289397.2:c.3335G>A NP_001276326.1:p.Arg1112Gln
NM_139045.4:c.3509G>A NP_620614.2:p.Arg1170Gln