Canonical Allele Identifier: CA4963795
Gene: SMARCA2 HGNC NCBI

Linked Data

dbSNP Id: rs780812007
gnomAD v2: 9-2115999-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2115999G>T , CM000671.2:g.2115999G>T GRCh38
NC_000009.11:g.2115999G>T , CM000671.1:g.2115999G>T GRCh37
NC_000009.10:g.2105999G>T NCBI36
NG_032162.1:g.105658G>T
NG_032162.2:g.140710G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3274G>T ENSP00000515861.1:p.Glu1092Ter
ENST00000704352.1:c.1174-45687G>T ENSP00000515863.1:n.1174-45687G>T
ENST00000704353.1:c.1174-45687G>T ENSP00000515864.1:n.1174-45687G>T
ENST00000704354.1:c.3618G>T
ENST00000704355.1:c.1998G>T
ENST00000349721.8:c.3634G>T MANE Select ENSP00000265773.5:p.Glu1212Ter
ENST00000357248.8:c.3634G>T ENSP00000349788.2:p.Glu1212Ter
ENST00000635739.1:n.2302G>T
ENST00000636157.1:n.1241G>T
ENST00000638139.1:n.668G>T
ENST00000349721.7:c.3634G>T ENSP00000265773.5:p.Glu1212Ter
ENST00000357248.7:c.3634G>T ENSP00000349788.2:p.Glu1212Ter
ENST00000382194.6:c.3634G>T ENSP00000371629.1:p.Glu1212Ter
ENST00000382203.5:c.3634G>T ENSP00000371638.1:p.Glu1212Ter
ENST00000450198.6:c.3460G>T ENSP00000392081.2:p.Glu1154Ter
ENST00000634760.1:c.3634G>T ENSP00000489256.1:p.Glu1212Ter
ENST00000634772.1:c.62-3459G>T
ENST00000634925.1:n.1125G>T
NM_001289396.1:c.3634G>T NP_001276325.1:p.Glu1212Ter
NM_001289397.1:c.3460G>T NP_001276326.1:p.Glu1154Ter
NM_003070.4:c.3634G>T NP_003061.3:p.Glu1212Ter
NM_139045.3:c.3634G>T NP_620614.2:p.Glu1212Ter
NM_003070.5:c.3634G>T MANE Select NP_003061.3:p.Glu1212Ter
NM_001289397.2:c.3460G>T NP_001276326.1:p.Glu1154Ter
NM_139045.4:c.3634G>T NP_620614.2:p.Glu1212Ter