Canonical Allele Identifier: CA1827951803
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2115932A= , CM000671.2:g.2115932A= GRCh38
NC_000009.11:g.2115932A= , CM000671.1:g.2115932A= GRCh37
NC_000009.10:g.2105932A= NCBI36
NG_032162.1:g.105591A=
NG_032162.2:g.140643A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.3207A= ENSP00000515861.1:p.Lys1069=
ENST00000704352.1:c.1174-45754A= ENSP00000515863.1:n.1174-45754A=
ENST00000704353.1:c.1174-45754A= ENSP00000515864.1:n.1174-45754A=
ENST00000704354.1:c.3551A=
ENST00000704355.1:c.1931A=
ENST00000349721.8:c.3567A= MANE Select ENSP00000265773.5:p.Lys1189=
ENST00000357248.8:c.3567A= ENSP00000349788.2:p.Lys1189=
ENST00000635739.1:n.2235A=
ENST00000636157.1:n.1174A=
ENST00000638139.1:n.601A=
ENST00000349721.7:c.3567A= ENSP00000265773.5:p.Lys1189=
ENST00000357248.7:c.3567A= ENSP00000349788.2:p.Lys1189=
ENST00000382194.6:c.3567A= ENSP00000371629.1:p.Lys1189=
ENST00000382203.5:c.3567A= ENSP00000371638.1:p.Lys1189=
ENST00000450198.6:c.3393A= ENSP00000392081.2:p.Lys1131=
ENST00000634760.1:c.3567A= ENSP00000489256.1:p.Lys1189=
ENST00000634772.1:c.62-3526A=
ENST00000634925.1:n.1058A=
NM_001289396.1:c.3567A= NP_001276325.1:p.Lys1189=
NM_001289397.1:c.3393A= NP_001276326.1:p.Lys1131=
NM_003070.4:c.3567A= NP_003061.3:p.Lys1189=
NM_139045.3:c.3567A= NP_620614.2:p.Lys1189=
NM_003070.5:c.3567A= MANE Select NP_003061.3:p.Lys1189=
NM_001289397.2:c.3393A= NP_001276326.1:p.Lys1131=
NM_139045.4:c.3567A= NP_620614.2:p.Lys1189=