Canonical Allele Identifier: CA372788741
Gene: SMARCA2 HGNC NCBI

Linked Data

gnomAD v4: 9-2115874-G-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000704350.1:c.3149G>C ENSP00000515861.1:p.Arg1050Pro
ENST00000704352.1:c.1174-45812G>C ENSP00000515863.1:n.1174-45812G>C
ENST00000704353.1:c.1174-45812G>C ENSP00000515864.1:n.1174-45812G>C
ENST00000704354.1:c.3493G>C
ENST00000704355.1:c.1873G>C
ENST00000349721.8:c.3509G>C MANE Select ENSP00000265773.5:p.Arg1170Pro
ENST00000357248.8:c.3509G>C ENSP00000349788.2:p.Arg1170Pro
ENST00000635739.1:n.2177G>C
ENST00000636157.1:n.1116G>C
ENST00000638139.1:n.543G>C
ENST00000349721.7:c.3509G>C ENSP00000265773.5:p.Arg1170Pro
ENST00000357248.7:c.3509G>C ENSP00000349788.2:p.Arg1170Pro
ENST00000382194.6:c.3509G>C ENSP00000371629.1:p.Arg1170Pro
ENST00000382203.5:c.3509G>C ENSP00000371638.1:p.Arg1170Pro
ENST00000450198.6:c.3335G>C ENSP00000392081.2:p.Arg1112Pro
ENST00000634760.1:c.3509G>C ENSP00000489256.1:p.Arg1170Pro
ENST00000634772.1:c.62-3584G>C
ENST00000634925.1:n.1000G>C
NM_001289396.1:c.3509G>C NP_001276325.1:p.Arg1170Pro
NM_001289397.1:c.3335G>C NP_001276326.1:p.Arg1112Pro
NM_003070.4:c.3509G>C NP_003061.3:p.Arg1170Pro
NM_139045.3:c.3509G>C NP_620614.2:p.Arg1170Pro
NM_003070.5:c.3509G>C MANE Select NP_003061.3:p.Arg1170Pro
NM_001289397.2:c.3335G>C NP_001276326.1:p.Arg1112Pro
NM_139045.4:c.3509G>C NP_620614.2:p.Arg1170Pro