Canonical Allele Identifier: CA1827938106
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2095958T= , CM000671.2:g.2095958T= GRCh38
NC_000009.11:g.2095958T= , CM000671.1:g.2095958T= GRCh37
NC_000009.10:g.2085958T= NCBI36
NG_032162.1:g.85617T=
NG_032162.2:g.120669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000637134.2:c.2884-699T= ENSP00000489667.2:n.2884-699T=
ENST00000704350.1:c.2524-699T= ENSP00000515861.1:n.2524-699T=
ENST00000704352.1:c.1173+41235T= ENSP00000515863.1:n.1173+41235T=
ENST00000704353.1:c.1173+41235T= ENSP00000515864.1:n.1173+41235T=
ENST00000704354.1:c.2868-699T=
ENST00000704355.1:c.1248-699T=
ENST00000349721.8:c.2884-699T= MANE Select ENSP00000265773.5:n.2884-699T=
ENST00000357248.8:c.2884-699T= ENSP00000349788.2:n.2884-699T=
ENST00000635739.1:n.1552-699T=
ENST00000636157.1:n.491-699T=
ENST00000349721.7:c.2884-699T= ENSP00000265773.5:n.2884-699T=
ENST00000357248.7:c.2884-699T= ENSP00000349788.2:n.2884-699T=
ENST00000382194.6:c.2884-699T= ENSP00000371629.1:n.2884-699T=
ENST00000382203.5:c.2884-699T= ENSP00000371638.1:n.2884-699T=
ENST00000450198.6:c.2710-699T= ENSP00000392081.2:n.2710-699T=
ENST00000634760.1:c.2884-699T= ENSP00000489256.1:n.2884-699T=
ENST00000634925.1:n.375-699T=
ENST00000635185.1:c.651-699T=
NM_001289396.1:c.2884-699T= NP_001276325.1:n.2884-699T=
NM_001289397.1:c.2710-699T= NP_001276326.1:n.2710-699T=
NM_003070.4:c.2884-699T= NP_003061.3:n.2884-699T=
NM_139045.3:c.2884-699T= NP_620614.2:n.2884-699T=
NM_003070.5:c.2884-699T= MANE Select NP_003061.3:n.2884-699T=
NM_001289397.2:c.2710-699T= NP_001276326.1:n.2710-699T=
NM_139045.4:c.2884-699T= NP_620614.2:n.2884-699T=