Canonical Allele Identifier: CA219896

Gene: SMARCA2

Linked Data

• ClinVar Variation Id: 68773
• ClinVar RCV Id: RCV000059679
• dbSNP Id: rs281875196
• MyVariant Identifiers: chr9:g.2115927G>C (hg19) ; chr9:g.2115927G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115927G>C , CM000671.2:g.2115927G>C	GRCh38
NC_000009.11:g.2115927G>C , CM000671.1:g.2115927G>C	GRCh37
NC_000009.10:g.2105927G>C	NCBI36
NG_032162.1:g.105586G>C
NG_032162.2:g.140638G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3202G>C	ENSP00000515861.1:p.Ala1068Pro
ENST00000704352.1:c.1174-45759G>C	ENSP00000515863.1:n.1174-45759G>C
ENST00000704353.1:c.1174-45759G>C	ENSP00000515864.1:n.1174-45759G>C
ENST00000704354.1:c.3546G>C
ENST00000704355.1:c.1926G>C
ENST00000349721.8:c.3562G>C MANE Select	ENSP00000265773.5:p.Ala1188Pro
ENST00000357248.8:c.3562G>C	ENSP00000349788.2:p.Ala1188Pro
ENST00000635739.1:n.2230G>C
ENST00000636157.1:n.1169G>C
ENST00000638139.1:n.596G>C
ENST00000349721.7:c.3562G>C	ENSP00000265773.5:p.Ala1188Pro
ENST00000357248.7:c.3562G>C	ENSP00000349788.2:p.Ala1188Pro
ENST00000382194.6:c.3562G>C	ENSP00000371629.1:p.Ala1188Pro
ENST00000382203.5:c.3562G>C	ENSP00000371638.1:p.Ala1188Pro
ENST00000450198.6:c.3388G>C	ENSP00000392081.2:p.Ala1130Pro
ENST00000634760.1:c.3562G>C	ENSP00000489256.1:p.Ala1188Pro
ENST00000634772.1:c.62-3531G>C
ENST00000634925.1:n.1053G>C
NM_001289396.1:c.3562G>C	NP_001276325.1:p.Ala1188Pro
NM_001289397.1:c.3388G>C	NP_001276326.1:p.Ala1130Pro
NM_003070.4:c.3562G>C	NP_003061.3:p.Ala1188Pro
NM_139045.3:c.3562G>C	NP_620614.2:p.Ala1188Pro
NM_003070.5:c.3562G>C MANE Select	NP_003061.3:p.Ala1188Pro
NM_001289397.2:c.3388G>C	NP_001276326.1:p.Ala1130Pro
NM_139045.4:c.3562G>C	NP_620614.2:p.Ala1188Pro