Canonical Allele Identifier: CA1827955804
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2123815G= , CM000671.2:g.2123815G= GRCh38
NC_000009.11:g.2123815G= , CM000671.1:g.2123815G= GRCh37
NC_000009.10:g.2113815G= NCBI36
NG_032162.1:g.113474G=
NG_032162.2:g.148526G=

Transcript Alleles

HGVS Amino-acid change
ENST00000704350.1:c.3499G= ENSP00000515861.1:p.Asp1167=
ENST00000704352.1:c.1174-37871G= ENSP00000515863.1:n.1174-37871G=
ENST00000704353.1:c.1174-37871G= ENSP00000515864.1:n.1174-37871G=
ENST00000704354.1:c.3843G=
ENST00000704355.1:c.2223G=
ENST00000349721.8:c.3859G= MANE Select ENSP00000265773.5:p.Asp1287=
ENST00000357248.8:c.3859G= ENSP00000349788.2:p.Asp1287=
ENST00000635739.1:n.2527G=
ENST00000636157.1:n.1466G=
ENST00000638139.1:n.893G=
ENST00000349721.7:c.3859G= ENSP00000265773.5:p.Asp1287=
ENST00000357248.7:c.3859G= ENSP00000349788.2:p.Asp1287=
ENST00000382194.6:c.3859G= ENSP00000371629.1:p.Asp1287=
ENST00000382203.5:c.3859G= ENSP00000371638.1:p.Asp1287=
ENST00000450198.6:c.3685G= ENSP00000392081.2:p.Asp1229=
ENST00000634760.1:c.3859G= ENSP00000489256.1:p.Asp1287=
ENST00000634772.1:c.236G=
ENST00000634925.1:n.1350G=
NM_001289396.1:c.3859G= NP_001276325.1:p.Asp1287=
NM_001289397.1:c.3685G= NP_001276326.1:p.Asp1229=
NM_003070.4:c.3859G= NP_003061.3:p.Asp1287=
NM_139045.3:c.3859G= NP_620614.2:p.Asp1287=
NM_003070.5:c.3859G= MANE Select NP_003061.3:p.Asp1287=
NM_001289397.2:c.3685G= NP_001276326.1:p.Asp1229=
NM_139045.4:c.3859G= NP_620614.2:p.Asp1287=