Canonical Allele Identifier: CA463711853

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2123808C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2123808C>A , CM000671.2:g.2123808C>A	GRCh38
NC_000009.11:g.2123808C>A , CM000671.1:g.2123808C>A	GRCh37
NC_000009.10:g.2113808C>A	NCBI36
NG_032162.1:g.113467C>A
NG_032162.2:g.148519C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704350.1:c.3492C>A	ENSP00000515861.1:p.Ile1164=
ENST00000704352.1:c.1174-37878C>A	ENSP00000515863.1:n.1174-37878C>A
ENST00000704353.1:c.1174-37878C>A	ENSP00000515864.1:n.1174-37878C>A
ENST00000704354.1:c.3836C>A
ENST00000704355.1:c.2216C>A
ENST00000349721.8:c.3852C>A MANE Select	ENSP00000265773.5:p.Ile1284=
ENST00000357248.8:c.3852C>A	ENSP00000349788.2:p.Ile1284=
ENST00000635739.1:n.2520C>A
ENST00000636157.1:n.1459C>A
ENST00000638139.1:n.886C>A
ENST00000349721.7:c.3852C>A	ENSP00000265773.5:p.Ile1284=
ENST00000357248.7:c.3852C>A	ENSP00000349788.2:p.Ile1284=
ENST00000382194.6:c.3852C>A	ENSP00000371629.1:p.Ile1284=
ENST00000382203.5:c.3852C>A	ENSP00000371638.1:p.Ile1284=
ENST00000450198.6:c.3678C>A	ENSP00000392081.2:p.Ile1226=
ENST00000634760.1:c.3852C>A	ENSP00000489256.1:p.Ile1284=
ENST00000634772.1:c.229C>A
ENST00000634925.1:n.1343C>A
NM_001289396.1:c.3852C>A	NP_001276325.1:p.Ile1284=
NM_001289397.1:c.3678C>A	NP_001276326.1:p.Ile1226=
NM_003070.4:c.3852C>A	NP_003061.3:p.Ile1284=
NM_139045.3:c.3852C>A	NP_620614.2:p.Ile1284=
NM_003070.5:c.3852C>A MANE Select	NP_003061.3:p.Ile1284=
NM_001289397.2:c.3678C>A	NP_001276326.1:p.Ile1226=
NM_139045.4:c.3852C>A	NP_620614.2:p.Ile1284=