Canonical Allele Identifier: CA372788666

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2115849C>G (hg19) ; chr9:g.2115849C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115849C>G , CM000671.2:g.2115849C>G	GRCh38
NC_000009.11:g.2115849C>G , CM000671.1:g.2115849C>G	GRCh37
NC_000009.10:g.2105849C>G	NCBI36
NG_032162.1:g.105508C>G
NG_032162.2:g.140560C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3124C>G	ENSP00000515861.1:p.Arg1042Gly
ENST00000704352.1:c.1174-45837C>G	ENSP00000515863.1:n.1174-45837C>G
ENST00000704353.1:c.1174-45837C>G	ENSP00000515864.1:n.1174-45837C>G
ENST00000704354.1:c.3468C>G
ENST00000704355.1:c.1848C>G
ENST00000349721.8:c.3484C>G MANE Select	ENSP00000265773.5:p.Arg1162Gly
ENST00000357248.8:c.3484C>G	ENSP00000349788.2:p.Arg1162Gly
ENST00000635739.1:n.2152C>G
ENST00000636157.1:n.1091C>G
ENST00000638139.1:n.518C>G
ENST00000349721.7:c.3484C>G	ENSP00000265773.5:p.Arg1162Gly
ENST00000357248.7:c.3484C>G	ENSP00000349788.2:p.Arg1162Gly
ENST00000382194.6:c.3484C>G	ENSP00000371629.1:p.Arg1162Gly
ENST00000382203.5:c.3484C>G	ENSP00000371638.1:p.Arg1162Gly
ENST00000450198.6:c.3310C>G	ENSP00000392081.2:p.Arg1104Gly
ENST00000634760.1:c.3484C>G	ENSP00000489256.1:p.Arg1162Gly
ENST00000634772.1:c.62-3609C>G
ENST00000634925.1:n.975C>G
NM_001289396.1:c.3484C>G	NP_001276325.1:p.Arg1162Gly
NM_001289397.1:c.3310C>G	NP_001276326.1:p.Arg1104Gly
NM_003070.4:c.3484C>G	NP_003061.3:p.Arg1162Gly
NM_139045.3:c.3484C>G	NP_620614.2:p.Arg1162Gly
NM_003070.5:c.3484C>G MANE Select	NP_003061.3:p.Arg1162Gly
NM_001289397.2:c.3310C>G	NP_001276326.1:p.Arg1104Gly
NM_139045.4:c.3484C>G	NP_620614.2:p.Arg1162Gly