Canonical Allele Identifier: CA1827951886
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2116163A= , CM000671.2:g.2116163A= GRCh38
NC_000009.11:g.2116163A= , CM000671.1:g.2116163A= GRCh37
NC_000009.10:g.2106163A= NCBI36
NG_032162.1:g.105822A=
NG_032162.2:g.140874A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3324+114A= ENSP00000515861.1:n.3324+114A=
ENST00000704352.1:c.1174-45523A= ENSP00000515863.1:n.1174-45523A=
ENST00000704353.1:c.1174-45523A= ENSP00000515864.1:n.1174-45523A=
ENST00000704354.1:c.3668+114A=
ENST00000704355.1:c.2048+114A=
ENST00000349721.8:c.3684+114A= MANE Select ENSP00000265773.5:n.3684+114A=
ENST00000357248.8:c.3684+114A= ENSP00000349788.2:n.3684+114A=
ENST00000635739.1:n.2352+114A=
ENST00000636157.1:n.1291+114A=
ENST00000638139.1:n.718+114A=
ENST00000349721.7:c.3684+114A= ENSP00000265773.5:n.3684+114A=
ENST00000357248.7:c.3684+114A= ENSP00000349788.2:n.3684+114A=
ENST00000382194.6:c.3684+114A= ENSP00000371629.1:n.3684+114A=
ENST00000382203.5:c.3684+114A= ENSP00000371638.1:n.3684+114A=
ENST00000450198.6:c.3510+114A= ENSP00000392081.2:n.3510+114A=
ENST00000634760.1:c.3684+114A= ENSP00000489256.1:n.3684+114A=
ENST00000634772.1:c.62-3295A=
ENST00000634925.1:n.1175+114A=
NM_001289396.1:c.3684+114A= NP_001276325.1:n.3684+114A=
NM_001289397.1:c.3510+114A= NP_001276326.1:n.3510+114A=
NM_003070.4:c.3684+114A= NP_003061.3:n.3684+114A=
NM_139045.3:c.3684+114A= NP_620614.2:n.3684+114A=
NM_003070.5:c.3684+114A= MANE Select NP_003061.3:n.3684+114A=
NM_001289397.2:c.3510+114A= NP_001276326.1:n.3510+114A=
NM_139045.4:c.3684+114A= NP_620614.2:n.3684+114A=