Canonical Allele Identifier: CA372790719

Gene: SMARCA2

Linked Data

• MyVariant Identifiers: chr9:g.2123878T>G (hg19) ; chr9:g.2123878T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2123878T>G , CM000671.2:g.2123878T>G	GRCh38
NC_000009.11:g.2123878T>G , CM000671.1:g.2123878T>G	GRCh37
NC_000009.10:g.2113878T>G	NCBI36
NG_032162.1:g.113537T>G
NG_032162.2:g.148589T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000704350.1:c.3562T>G	ENSP00000515861.1:p.Ser1188Ala
ENST00000704352.1:c.1174-37808T>G	ENSP00000515863.1:n.1174-37808T>G
ENST00000704353.1:c.1174-37808T>G	ENSP00000515864.1:n.1174-37808T>G
ENST00000704354.1:c.3906T>G
ENST00000704355.1:c.2286T>G
ENST00000349721.8:c.3922T>G MANE Select	ENSP00000265773.5:p.Ser1308Ala
ENST00000357248.8:c.3922T>G	ENSP00000349788.2:p.Ser1308Ala
ENST00000635739.1:n.2590T>G
ENST00000636157.1:n.1529T>G
ENST00000638139.1:n.956T>G
ENST00000639760.2:c.29T>G
ENST00000349721.7:c.3922T>G	ENSP00000265773.5:p.Ser1308Ala
ENST00000357248.7:c.3922T>G	ENSP00000349788.2:p.Ser1308Ala
ENST00000382194.6:c.3922T>G	ENSP00000371629.1:p.Ser1308Ala
ENST00000382203.5:c.3922T>G	ENSP00000371638.1:p.Ser1308Ala
ENST00000450198.6:c.3748T>G	ENSP00000392081.2:p.Ser1250Ala
ENST00000634760.1:c.3922T>G	ENSP00000489256.1:p.Ser1308Ala
ENST00000634772.1:c.299T>G
ENST00000634925.1:n.1413T>G
NM_001289396.1:c.3922T>G	NP_001276325.1:p.Ser1308Ala
NM_001289397.1:c.3748T>G	NP_001276326.1:p.Ser1250Ala
NM_003070.4:c.3922T>G	NP_003061.3:p.Ser1308Ala
NM_139045.3:c.3922T>G	NP_620614.2:p.Ser1308Ala
NM_003070.5:c.3922T>G MANE Select	NP_003061.3:p.Ser1308Ala
NM_001289397.2:c.3748T>G	NP_001276326.1:p.Ser1250Ala
NM_139045.4:c.3922T>G	NP_620614.2:p.Ser1308Ala