Canonical Allele Identifier: CA2579289611
Gene: SMARCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2123708A>T , CM000671.2:g.2123708A>T GRCh38
NC_000009.11:g.2123708A>T , CM000671.1:g.2123708A>T GRCh37
NC_000009.10:g.2113708A>T NCBI36
NG_032162.1:g.113367A>T
NG_032162.2:g.148419A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000704350.1:c.3403-11A>T ENSP00000515861.1:n.3403-11A>T
ENST00000704352.1:c.1174-37978A>T ENSP00000515863.1:n.1174-37978A>T
ENST00000704353.1:c.1174-37978A>T ENSP00000515864.1:n.1174-37978A>T
ENST00000704354.1:c.3747-11A>T
ENST00000704355.1:c.2127-11A>T
ENST00000349721.8:c.3763-11A>T MANE Select ENSP00000265773.5:n.3763-11A>T
ENST00000357248.8:c.3763-11A>T ENSP00000349788.2:n.3763-11A>T
ENST00000635739.1:n.2431-11A>T
ENST00000636157.1:n.1370-11A>T
ENST00000638139.1:n.797-11A>T
ENST00000349721.7:c.3763-11A>T ENSP00000265773.5:n.3763-11A>T
ENST00000357248.7:c.3763-11A>T ENSP00000349788.2:n.3763-11A>T
ENST00000382194.6:c.3763-11A>T ENSP00000371629.1:n.3763-11A>T
ENST00000382203.5:c.3763-11A>T ENSP00000371638.1:n.3763-11A>T
ENST00000450198.6:c.3589-11A>T ENSP00000392081.2:n.3589-11A>T
ENST00000634760.1:c.3763-11A>T ENSP00000489256.1:n.3763-11A>T
ENST00000634772.1:c.140-11A>T
ENST00000634925.1:n.1254-11A>T
NM_001289396.1:c.3763-11A>T NP_001276325.1:n.3763-11A>T
NM_001289397.1:c.3589-11A>T NP_001276326.1:n.3589-11A>T
NM_003070.4:c.3763-11A>T NP_003061.3:n.3763-11A>T
NM_139045.3:c.3763-11A>T NP_620614.2:n.3763-11A>T
NM_003070.5:c.3763-11A>T MANE Select NP_003061.3:n.3763-11A>T
NM_001289397.2:c.3589-11A>T NP_001276326.1:n.3589-11A>T
NM_139045.4:c.3763-11A>T NP_620614.2:n.3763-11A>T