Canonical Allele Identifier: CA366234677

Gene: ARID1B

Linked Data

• dbSNP Id: rs1409112361
• MyVariant Identifiers: chr6:g.157511182A>G (hg19) ; chr6:g.157190048A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190048A>G , CM000668.2:g.157190048A>G	GRCh38
NC_000006.11:g.157511182A>G , CM000668.1:g.157511182A>G	GRCh37
NC_000006.10:g.157552874A>G	NCBI36
NG_032093.1:g.417119A>G
NG_032093.2:g.417119A>G
NG_066624.1:g.419023A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3910A>G	ENSP00000055163.8:p.Ile1304Val
ENST00000414678.8:c.3979A>G	ENSP00000412835.3:p.Ile1327Val
ENST00000637015.2:c.4198A>G	ENSP00000489729.2:p.Ile1400Val
ENST00000346085.10:c.3949A>G	ENSP00000344546.5:p.Ile1317Val
ENST00000350026.10:c.3661A>G	ENSP00000055163.7:p.Ile1221Val
ENST00000414678.7:c.2227A>G	ENSP00000412835.2:p.Ile743Val
ENST00000635849.1:c.1390A>G	ENSP00000490948.1:p.Ile464Val
ENST00000635957.1:c.1021A>G	ENSP00000490385.1:p.Ile341Val
ENST00000636930.2:c.4069A>G MANE Select	ENSP00000490491.2:p.Ile1357Val
ENST00000636940.1:n.2066A>G
ENST00000637015.1:c.1437A>G
ENST00000637568.1:c.1351A>G
ENST00000637741.1:n.735A>G
ENST00000637810.1:c.1411A>G	ENSP00000489636.1:p.Ile471Val
ENST00000637904.1:c.1570A>G	ENSP00000490550.1:p.Ile524Val
ENST00000647938.1:c.3700A>G	ENSP00000498155.1:p.Ile1234Val
ENST00000346085.9:c.3700A>G	ENSP00000344546.4:p.Ile1234Val
ENST00000350026.9:c.3661A>G	ENSP00000055163.7:p.Ile1221Val
ENST00000414678.6:c.2227A>G	ENSP00000412835.2:p.Ile743Val
NM_017519.2:c.3661A>G	NP_059989.2:p.Ile1221Val
NM_020732.3:c.3700A>G	NP_065783.3:p.Ile1234Val
XM_005267069.3:c.3820A>G	XP_005267126.2:p.Ile1274Val
XM_011535984.1:c.2899A>G	XP_011534286.1:p.Ile967Val
XM_011535985.1:c.2719A>G	XP_011534287.1:p.Ile907Val
XM_011535986.1:c.2479A>G	XP_011534288.1:p.Ile827Val
XM_011535987.1:c.2098A>G	XP_011534289.1:p.Ile700Val
XM_011535988.1:c.961A>G	XP_011534290.1:p.Ile321Val
NM_001346813.1:c.3820A>G	NP_001333742.1:p.Ile1274Val
NM_001363725.1:c.1570A>G	NP_001350654.1:p.Ile524Val
XM_011535984.2:c.4030A>G	XP_011534286.2:p.Ile1344Val
XM_011535988.3:c.961A>G	XP_011534290.1:p.Ile321Val
XM_017011103.2:c.3931A>G	XP_016866592.1:p.Ile1311Val
XM_017011104.1:c.3901A>G	XP_016866593.1:p.Ile1301Val
XM_017011105.2:c.3871A>G	XP_016866594.1:p.Ile1291Val
XM_017011106.2:c.3742A>G	XP_016866595.1:p.Ile1248Val
XM_017011107.2:c.3721A>G	XP_016866596.1:p.Ile1241Val
XR_002956289.1:n.4113A>G
NM_001363725.2:c.1570A>G	NP_001350654.1:p.Ile524Val
NM_001371656.1:c.3949A>G	NP_001358585.1:p.Ile1317Val
NM_001374820.1:c.3949A>G	NP_001361749.1:p.Ile1317Val
NM_001374828.1:c.4069A>G MANE Select	NP_001361757.1:p.Ile1357Val
NM_017519.3:c.3910A>G	NP_059989.3:p.Ile1304Val