Canonical Allele Identifier: CA1827955803
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2123811T= , CM000671.2:g.2123811T= GRCh38
NC_000009.11:g.2123811T= , CM000671.1:g.2123811T= GRCh37
NC_000009.10:g.2113811T= NCBI36
NG_032162.1:g.113470T=
NG_032162.2:g.148522T=

Transcript Alleles

HGVS Amino-acid change
ENST00000704350.1:c.3495T= ENSP00000515861.1:p.Ile1165=
ENST00000704352.1:c.1174-37875T= ENSP00000515863.1:n.1174-37875T=
ENST00000704353.1:c.1174-37875T= ENSP00000515864.1:n.1174-37875T=
ENST00000704354.1:c.3839T=
ENST00000704355.1:c.2219T=
ENST00000349721.8:c.3855T= MANE Select ENSP00000265773.5:p.Ile1285=
ENST00000357248.8:c.3855T= ENSP00000349788.2:p.Ile1285=
ENST00000635739.1:n.2523T=
ENST00000636157.1:n.1462T=
ENST00000638139.1:n.889T=
ENST00000349721.7:c.3855T= ENSP00000265773.5:p.Ile1285=
ENST00000357248.7:c.3855T= ENSP00000349788.2:p.Ile1285=
ENST00000382194.6:c.3855T= ENSP00000371629.1:p.Ile1285=
ENST00000382203.5:c.3855T= ENSP00000371638.1:p.Ile1285=
ENST00000450198.6:c.3681T= ENSP00000392081.2:p.Ile1227=
ENST00000634760.1:c.3855T= ENSP00000489256.1:p.Ile1285=
ENST00000634772.1:c.232T=
ENST00000634925.1:n.1346T=
NM_001289396.1:c.3855T= NP_001276325.1:p.Ile1285=
NM_001289397.1:c.3681T= NP_001276326.1:p.Ile1227=
NM_003070.4:c.3855T= NP_003061.3:p.Ile1285=
NM_139045.3:c.3855T= NP_620614.2:p.Ile1285=
NM_003070.5:c.3855T= MANE Select NP_003061.3:p.Ile1285=
NM_001289397.2:c.3681T= NP_001276326.1:p.Ile1227=
NM_139045.4:c.3855T= NP_620614.2:p.Ile1285=