Canonical Allele Identifier: CA366241976

Gene: ARID1B

Linked Data

• dbSNP Id: rs1583501651
• MyVariant Identifiers: chr6:g.157522230T>G (hg19) ; chr6:g.157201096T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201096T>G , CM000668.2:g.157201096T>G	GRCh38
NC_000006.11:g.157522230T>G , CM000668.1:g.157522230T>G	GRCh37
NC_000006.10:g.157563922T>G	NCBI36
NG_032093.1:g.428167T>G
NG_032093.2:g.428167T>G
NG_066624.1:g.430071T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4712T>G	ENSP00000055163.8:p.Val1571Gly
ENST00000414678.8:c.4781T>G	ENSP00000412835.3:p.Val1594Gly
ENST00000637015.2:c.5000T>G	ENSP00000489729.2:p.Val1667Gly
ENST00000346085.10:c.4751T>G	ENSP00000344546.5:p.Val1584Gly
ENST00000350026.10:c.4463T>G	ENSP00000055163.7:p.Val1488Gly
ENST00000414678.7:c.3029T>G	ENSP00000412835.2:p.Val1010Gly
ENST00000635849.1:c.2192T>G	ENSP00000490948.1:p.Val731Gly
ENST00000635957.1:c.1823T>G	ENSP00000490385.1:p.Val608Gly
ENST00000636227.1:n.3334T>G
ENST00000636254.1:n.791T>G
ENST00000636930.2:c.4871T>G MANE Select	ENSP00000490491.2:p.Val1624Gly
ENST00000636940.1:n.2868T>G
ENST00000637015.1:c.2239T>G
ENST00000637568.1:c.2153T>G
ENST00000637741.1:n.1537T>G
ENST00000637810.1:c.2213T>G	ENSP00000489636.1:p.Val738Gly
ENST00000637904.1:c.2372T>G	ENSP00000490550.1:p.Val791Gly
ENST00000647938.1:c.4502T>G	ENSP00000498155.1:p.Val1501Gly
ENST00000346085.9:c.4502T>G	ENSP00000344546.4:p.Val1501Gly
ENST00000350026.9:c.4463T>G	ENSP00000055163.7:p.Val1488Gly
ENST00000414678.6:c.3029T>G	ENSP00000412835.2:p.Val1010Gly
NM_017519.2:c.4463T>G	NP_059989.2:p.Val1488Gly
NM_020732.3:c.4502T>G	NP_065783.3:p.Val1501Gly
XM_005267069.3:c.4622T>G	XP_005267126.2:p.Val1541Gly
XM_011535984.1:c.3701T>G	XP_011534286.1:p.Val1234Gly
XM_011535985.1:c.3521T>G	XP_011534287.1:p.Val1174Gly
XM_011535986.1:c.3281T>G	XP_011534288.1:p.Val1094Gly
XM_011535987.1:c.2900T>G	XP_011534289.1:p.Val967Gly
XM_011535988.1:c.1763T>G	XP_011534290.1:p.Val588Gly
NM_001346813.1:c.4622T>G	NP_001333742.1:p.Val1541Gly
NM_001363725.1:c.2372T>G	NP_001350654.1:p.Val791Gly
XM_011535984.2:c.4832T>G	XP_011534286.2:p.Val1611Gly
XM_011535988.3:c.1763T>G	XP_011534290.1:p.Val588Gly
XM_017011103.2:c.4733T>G	XP_016866592.1:p.Val1578Gly
XM_017011104.1:c.4703T>G	XP_016866593.1:p.Val1568Gly
XM_017011105.2:c.4673T>G	XP_016866594.1:p.Val1558Gly
XM_017011106.2:c.4544T>G	XP_016866595.1:p.Val1515Gly
XM_017011107.2:c.4523T>G	XP_016866596.1:p.Val1508Gly
XR_002956289.1:n.4818T>G
NM_001363725.2:c.2372T>G	NP_001350654.1:p.Val791Gly
NM_001371656.1:c.4751T>G	NP_001358585.1:p.Val1584Gly
NM_001374820.1:c.4751T>G	NP_001361749.1:p.Val1584Gly
NM_001374828.1:c.4871T>G MANE Select	NP_001361757.1:p.Val1624Gly
NM_017519.3:c.4712T>G	NP_059989.3:p.Val1571Gly