Canonical Allele Identifier: CA463852681

Gene: SMARCA2

Linked Data

• gnomAD v4: 9-2115848-C-T
• MyVariant Identifiers: chr9:g.2115848C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115848C>T , CM000671.2:g.2115848C>T	GRCh38
NC_000009.11:g.2115848C>T , CM000671.1:g.2115848C>T	GRCh37
NC_000009.10:g.2105848C>T	NCBI36
NG_032162.1:g.105507C>T
NG_032162.2:g.140559C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3123C>T	ENSP00000515861.1:p.His1041=
ENST00000704352.1:c.1174-45838C>T	ENSP00000515863.1:n.1174-45838C>T
ENST00000704353.1:c.1174-45838C>T	ENSP00000515864.1:n.1174-45838C>T
ENST00000704354.1:c.3467C>T
ENST00000704355.1:c.1847C>T
ENST00000349721.8:c.3483C>T MANE Select	ENSP00000265773.5:p.His1161=
ENST00000357248.8:c.3483C>T	ENSP00000349788.2:p.His1161=
ENST00000635739.1:n.2151C>T
ENST00000636157.1:n.1090C>T
ENST00000638139.1:n.517C>T
ENST00000349721.7:c.3483C>T	ENSP00000265773.5:p.His1161=
ENST00000357248.7:c.3483C>T	ENSP00000349788.2:p.His1161=
ENST00000382194.6:c.3483C>T	ENSP00000371629.1:p.His1161=
ENST00000382203.5:c.3483C>T	ENSP00000371638.1:p.His1161=
ENST00000450198.6:c.3309C>T	ENSP00000392081.2:p.His1103=
ENST00000634760.1:c.3483C>T	ENSP00000489256.1:p.His1161=
ENST00000634772.1:c.62-3610C>T
ENST00000634925.1:n.974C>T
NM_001289396.1:c.3483C>T	NP_001276325.1:p.His1161=
NM_001289397.1:c.3309C>T	NP_001276326.1:p.His1103=
NM_003070.4:c.3483C>T	NP_003061.3:p.His1161=
NM_139045.3:c.3483C>T	NP_620614.2:p.His1161=
NM_003070.5:c.3483C>T MANE Select	NP_003061.3:p.His1161=
NM_001289397.2:c.3309C>T	NP_001276326.1:p.His1103=
NM_139045.4:c.3483C>T	NP_620614.2:p.His1161=