Canonical Allele Identifier: CA463852668

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2115833C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115833C>G , CM000671.2:g.2115833C>G	GRCh38
NC_000009.11:g.2115833C>G , CM000671.1:g.2115833C>G	GRCh37
NC_000009.10:g.2105833C>G	NCBI36
NG_032162.1:g.105492C>G
NG_032162.2:g.140544C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3108C>G	ENSP00000515861.1:p.Ala1036=
ENST00000704352.1:c.1174-45853C>G	ENSP00000515863.1:n.1174-45853C>G
ENST00000704353.1:c.1174-45853C>G	ENSP00000515864.1:n.1174-45853C>G
ENST00000704354.1:c.3452C>G
ENST00000704355.1:c.1832C>G
ENST00000349721.8:c.3468C>G MANE Select	ENSP00000265773.5:p.Ala1156=
ENST00000357248.8:c.3468C>G	ENSP00000349788.2:p.Ala1156=
ENST00000635739.1:n.2136C>G
ENST00000636157.1:n.1075C>G
ENST00000638139.1:n.502C>G
ENST00000349721.7:c.3468C>G	ENSP00000265773.5:p.Ala1156=
ENST00000357248.7:c.3468C>G	ENSP00000349788.2:p.Ala1156=
ENST00000382194.6:c.3468C>G	ENSP00000371629.1:p.Ala1156=
ENST00000382203.5:c.3468C>G	ENSP00000371638.1:p.Ala1156=
ENST00000450198.6:c.3294C>G	ENSP00000392081.2:p.Ala1098=
ENST00000634760.1:c.3468C>G	ENSP00000489256.1:p.Ala1156=
ENST00000634772.1:c.62-3625C>G
ENST00000634925.1:n.959C>G
NM_001289396.1:c.3468C>G	NP_001276325.1:p.Ala1156=
NM_001289397.1:c.3294C>G	NP_001276326.1:p.Ala1098=
NM_003070.4:c.3468C>G	NP_003061.3:p.Ala1156=
NM_139045.3:c.3468C>G	NP_620614.2:p.Ala1156=
NM_003070.5:c.3468C>G MANE Select	NP_003061.3:p.Ala1156=
NM_001289397.2:c.3294C>G	NP_001276326.1:p.Ala1098=
NM_139045.4:c.3468C>G	NP_620614.2:p.Ala1156=