Canonical Allele Identifier: CA1827938109
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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