Canonical Allele Identifier: CA366234817

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511193C>G (hg19) ; chr6:g.157190059C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190059C>G , CM000668.2:g.157190059C>G	GRCh38
NC_000006.11:g.157511193C>G , CM000668.1:g.157511193C>G	GRCh37
NC_000006.10:g.157552885C>G	NCBI36
NG_032093.1:g.417130C>G
NG_032093.2:g.417130C>G
NG_066624.1:g.419034C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3921C>G	ENSP00000055163.8:p.His1307Gln
ENST00000414678.8:c.3990C>G	ENSP00000412835.3:p.His1330Gln
ENST00000637015.2:c.4209C>G	ENSP00000489729.2:p.His1403Gln
ENST00000346085.10:c.3960C>G	ENSP00000344546.5:p.His1320Gln
ENST00000350026.10:c.3672C>G	ENSP00000055163.7:p.His1224Gln
ENST00000414678.7:c.2238C>G	ENSP00000412835.2:p.His746Gln
ENST00000635849.1:c.1401C>G	ENSP00000490948.1:p.His467Gln
ENST00000635957.1:c.1032C>G	ENSP00000490385.1:p.His344Gln
ENST00000636930.2:c.4080C>G MANE Select	ENSP00000490491.2:p.His1360Gln
ENST00000636940.1:n.2077C>G
ENST00000637015.1:c.1448C>G
ENST00000637568.1:c.1362C>G
ENST00000637741.1:n.746C>G
ENST00000637810.1:c.1422C>G	ENSP00000489636.1:p.His474Gln
ENST00000637904.1:c.1581C>G	ENSP00000490550.1:p.His527Gln
ENST00000647938.1:c.3711C>G	ENSP00000498155.1:p.His1237Gln
ENST00000346085.9:c.3711C>G	ENSP00000344546.4:p.His1237Gln
ENST00000350026.9:c.3672C>G	ENSP00000055163.7:p.His1224Gln
ENST00000414678.6:c.2238C>G	ENSP00000412835.2:p.His746Gln
NM_017519.2:c.3672C>G	NP_059989.2:p.His1224Gln
NM_020732.3:c.3711C>G	NP_065783.3:p.His1237Gln
XM_005267069.3:c.3831C>G	XP_005267126.2:p.His1277Gln
XM_011535984.1:c.2910C>G	XP_011534286.1:p.His970Gln
XM_011535985.1:c.2730C>G	XP_011534287.1:p.His910Gln
XM_011535986.1:c.2490C>G	XP_011534288.1:p.His830Gln
XM_011535987.1:c.2109C>G	XP_011534289.1:p.His703Gln
XM_011535988.1:c.972C>G	XP_011534290.1:p.His324Gln
NM_001346813.1:c.3831C>G	NP_001333742.1:p.His1277Gln
NM_001363725.1:c.1581C>G	NP_001350654.1:p.His527Gln
XM_011535984.2:c.4041C>G	XP_011534286.2:p.His1347Gln
XM_011535988.3:c.972C>G	XP_011534290.1:p.His324Gln
XM_017011103.2:c.3942C>G	XP_016866592.1:p.His1314Gln
XM_017011104.1:c.3912C>G	XP_016866593.1:p.His1304Gln
XM_017011105.2:c.3882C>G	XP_016866594.1:p.His1294Gln
XM_017011106.2:c.3753C>G	XP_016866595.1:p.His1251Gln
XM_017011107.2:c.3732C>G	XP_016866596.1:p.His1244Gln
XR_002956289.1:n.4124C>G
NM_001363725.2:c.1581C>G	NP_001350654.1:p.His527Gln
NM_001371656.1:c.3960C>G	NP_001358585.1:p.His1320Gln
NM_001374820.1:c.3960C>G	NP_001361749.1:p.His1320Gln
NM_001374828.1:c.4080C>G MANE Select	NP_001361757.1:p.His1360Gln
NM_017519.3:c.3921C>G	NP_059989.3:p.His1307Gln