Canonical Allele Identifier: CA463711833
Gene: SMARCA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2191291G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2191291G>A , CM000671.2:g.2191291G>A GRCh38
NC_000009.11:g.2191291G>A , CM000671.1:g.2191291G>A GRCh37
NC_000009.10:g.2181291G>A NCBI36
NG_032162.1:g.180950G>A
NG_032162.2:g.216002G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704350.1:c.4206G>A ENSP00000515861.1:p.Lys1402=
ENST00000704352.1:c.1758G>A ENSP00000515863.1:p.Lys586=
ENST00000704353.1:c.1812G>A ENSP00000515864.1:p.Lys604=
ENST00000704354.1:c.4550G>A
ENST00000704355.1:c.2930G>A
ENST00000349721.8:c.4620G>A MANE Select ENSP00000265773.5:p.Lys1540=
ENST00000357248.8:c.4566G>A ENSP00000349788.2:p.Lys1522=
ENST00000635739.1:n.3234G>A
ENST00000636157.1:n.2173G>A
ENST00000636367.1:c.*416G>A ENSP00000489942.1:n.*416G>A
ENST00000638139.1:n.1654G>A
ENST00000639760.2:c.673G>A
ENST00000302401.8:c.684G>A ENSP00000305411.3:p.Lys228=
ENST00000324954.10:c.594G>A ENSP00000324770.6:p.Lys198=
ENST00000349721.7:c.4620G>A ENSP00000265773.5:p.Lys1540=
ENST00000357248.7:c.4566G>A ENSP00000349788.2:p.Lys1522=
ENST00000382183.6:c.558G>A ENSP00000371618.1:p.Lys186=
ENST00000382185.6:c.678G>A ENSP00000371620.2:p.Lys226=
ENST00000382186.6:c.612G>A ENSP00000371621.1:p.Lys204=
ENST00000382194.6:c.4566G>A ENSP00000371629.1:p.Lys1522=
ENST00000382203.5:c.4620G>A ENSP00000371638.1:p.Lys1540=
ENST00000416751.2:c.558G>A ENSP00000412242.2:p.Lys186=
ENST00000417599.6:c.678G>A ENSP00000387486.2:p.Lys226=
ENST00000423555.6:c.678G>A ENSP00000413057.2:p.Lys226=
ENST00000450198.6:c.4392G>A ENSP00000392081.2:p.Lys1464=
ENST00000634338.1:c.732G>A ENSP00000489388.1:p.Lys244=
ENST00000634435.1:c.732G>A ENSP00000489212.1:p.Lys244=
ENST00000634760.1:c.*227G>A ENSP00000489256.1:n.*227G>A
ENST00000634781.1:c.630G>A ENSP00000489302.1:p.Lys210=
ENST00000634931.1:c.612G>A ENSP00000489433.1:p.Lys204=
ENST00000634989.1:c.*416G>A ENSP00000489100.1:n.*416G>A
ENST00000635273.1:n.462G>A
ENST00000635388.1:c.558G>A ENSP00000489271.1:p.Lys186=
ENST00000635530.1:c.678G>A ENSP00000489204.1:p.Lys226=
ENST00000635590.1:c.*416G>A ENSP00000489587.1:n.*416G>A
ENST00000635659.1:c.711G>A
NM_001289396.1:c.4620G>A NP_001276325.1:p.Lys1540=
NM_001289397.1:c.4392G>A NP_001276326.1:p.Lys1464=
NM_001289398.1:c.594G>A NP_001276327.1:p.Lys198=
NM_001289399.1:c.678G>A NP_001276328.1:p.Lys226=
NM_001289400.1:c.684G>A NP_001276329.1:p.Lys228=
NM_003070.4:c.4620G>A NP_003061.3:p.Lys1540=
NM_139045.3:c.4566G>A NP_620614.2:p.Lys1522=
XR_001746600.1:n.1362-10269C>T
XR_001746601.1:n.1316-10269C>T
NM_003070.5:c.4620G>A MANE Select NP_003061.3:p.Lys1540=
NM_001289397.2:c.4392G>A NP_001276326.1:p.Lys1464=
NM_001289398.2:c.594G>A NP_001276327.1:p.Lys198=
NM_139045.4:c.4566G>A NP_620614.2:p.Lys1522=