Canonical Allele Identifier: CA372789072

Gene: SMARCA2

Linked Data

• dbSNP Id: rs1206702590
• gnomAD v2: 9-2116021-C-T
• gnomAD v4: 9-2116021-C-T
• MyVariant Identifiers: chr9:g.2116021C>T (hg19) ; chr9:g.2116021C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2116021C>T , CM000671.2:g.2116021C>T	GRCh38
NC_000009.11:g.2116021C>T , CM000671.1:g.2116021C>T	GRCh37
NC_000009.10:g.2106021C>T	NCBI36
NG_032162.1:g.105680C>T
NG_032162.2:g.140732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3296C>T	ENSP00000515861.1:p.Ala1099Val
ENST00000704352.1:c.1174-45665C>T	ENSP00000515863.1:n.1174-45665C>T
ENST00000704353.1:c.1174-45665C>T	ENSP00000515864.1:n.1174-45665C>T
ENST00000704354.1:c.3640C>T
ENST00000704355.1:c.2020C>T
ENST00000349721.8:c.3656C>T MANE Select	ENSP00000265773.5:p.Ala1219Val
ENST00000357248.8:c.3656C>T	ENSP00000349788.2:p.Ala1219Val
ENST00000635739.1:n.2324C>T
ENST00000636157.1:n.1263C>T
ENST00000638139.1:n.690C>T
ENST00000349721.7:c.3656C>T	ENSP00000265773.5:p.Ala1219Val
ENST00000357248.7:c.3656C>T	ENSP00000349788.2:p.Ala1219Val
ENST00000382194.6:c.3656C>T	ENSP00000371629.1:p.Ala1219Val
ENST00000382203.5:c.3656C>T	ENSP00000371638.1:p.Ala1219Val
ENST00000450198.6:c.3482C>T	ENSP00000392081.2:p.Ala1161Val
ENST00000634760.1:c.3656C>T	ENSP00000489256.1:p.Ala1219Val
ENST00000634772.1:c.62-3437C>T
ENST00000634925.1:n.1147C>T
NM_001289396.1:c.3656C>T	NP_001276325.1:p.Ala1219Val
NM_001289397.1:c.3482C>T	NP_001276326.1:p.Ala1161Val
NM_003070.4:c.3656C>T	NP_003061.3:p.Ala1219Val
NM_139045.3:c.3656C>T	NP_620614.2:p.Ala1219Val
NM_003070.5:c.3656C>T MANE Select	NP_003061.3:p.Ala1219Val
NM_001289397.2:c.3482C>T	NP_001276326.1:p.Ala1161Val
NM_139045.4:c.3656C>T	NP_620614.2:p.Ala1219Val