Canonical Allele Identifier: CA463711902
Gene: SMARCA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2123877G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2123877G>A , CM000671.2:g.2123877G>A GRCh38
NC_000009.11:g.2123877G>A , CM000671.1:g.2123877G>A GRCh37
NC_000009.10:g.2113877G>A NCBI36
NG_032162.1:g.113536G>A
NG_032162.2:g.148588G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000704350.1:c.3561G>A ENSP00000515861.1:p.Gly1187=
ENST00000704352.1:c.1174-37809G>A ENSP00000515863.1:n.1174-37809G>A
ENST00000704353.1:c.1174-37809G>A ENSP00000515864.1:n.1174-37809G>A
ENST00000704354.1:c.3905G>A
ENST00000704355.1:c.2285G>A
ENST00000349721.8:c.3921G>A MANE Select ENSP00000265773.5:p.Gly1307=
ENST00000357248.8:c.3921G>A ENSP00000349788.2:p.Gly1307=
ENST00000635739.1:n.2589G>A
ENST00000636157.1:n.1528G>A
ENST00000638139.1:n.955G>A
ENST00000639760.2:c.28G>A
ENST00000349721.7:c.3921G>A ENSP00000265773.5:p.Gly1307=
ENST00000357248.7:c.3921G>A ENSP00000349788.2:p.Gly1307=
ENST00000382194.6:c.3921G>A ENSP00000371629.1:p.Gly1307=
ENST00000382203.5:c.3921G>A ENSP00000371638.1:p.Gly1307=
ENST00000450198.6:c.3747G>A ENSP00000392081.2:p.Gly1249=
ENST00000634760.1:c.3921G>A ENSP00000489256.1:p.Gly1307=
ENST00000634772.1:c.298G>A
ENST00000634925.1:n.1412G>A
NM_001289396.1:c.3921G>A NP_001276325.1:p.Gly1307=
NM_001289397.1:c.3747G>A NP_001276326.1:p.Gly1249=
NM_003070.4:c.3921G>A NP_003061.3:p.Gly1307=
NM_139045.3:c.3921G>A NP_620614.2:p.Gly1307=
NM_003070.5:c.3921G>A MANE Select NP_003061.3:p.Gly1307=
NM_001289397.2:c.3747G>A NP_001276326.1:p.Gly1249=
NM_139045.4:c.3921G>A NP_620614.2:p.Gly1307=