Canonical Allele Identifier: CA4067528

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1490013
• ClinVar RCV Id: RCV001978463
• dbSNP Id: rs138784762
• ExAC: 6:157511242 A / G
• gnomAD v2: 6-157511242-A-G
• gnomAD v3: 6-157190108-A-G
• gnomAD v4: 6-157190108-A-G
• MyVariant Identifiers: chr6:g.157511242A>G (hg19) ; chr6:g.157190108A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190108A>G , CM000668.2:g.157190108A>G	GRCh38
NC_000006.11:g.157511242A>G , CM000668.1:g.157511242A>G	GRCh37
NC_000006.10:g.157552934A>G	NCBI36
NG_032093.1:g.417179A>G
NG_032093.2:g.417179A>G
NG_066624.1:g.419083A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3970A>G	ENSP00000055163.8:p.Met1324Val
ENST00000414678.8:c.4039A>G	ENSP00000412835.3:p.Met1347Val
ENST00000637015.2:c.4258A>G	ENSP00000489729.2:p.Met1420Val
ENST00000346085.10:c.4009A>G	ENSP00000344546.5:p.Met1337Val
ENST00000350026.10:c.3721A>G	ENSP00000055163.7:p.Met1241Val
ENST00000414678.7:c.2287A>G	ENSP00000412835.2:p.Met763Val
ENST00000635849.1:c.1450A>G	ENSP00000490948.1:p.Met484Val
ENST00000635957.1:c.1081A>G	ENSP00000490385.1:p.Met361Val
ENST00000636930.2:c.4129A>G MANE Select	ENSP00000490491.2:p.Met1377Val
ENST00000636940.1:n.2126A>G
ENST00000637015.1:c.1497A>G
ENST00000637568.1:c.1411A>G
ENST00000637741.1:n.795A>G
ENST00000637810.1:c.1471A>G	ENSP00000489636.1:p.Met491Val
ENST00000637904.1:c.1630A>G	ENSP00000490550.1:p.Met544Val
ENST00000647938.1:c.3760A>G	ENSP00000498155.1:p.Met1254Val
ENST00000346085.9:c.3760A>G	ENSP00000344546.4:p.Met1254Val
ENST00000350026.9:c.3721A>G	ENSP00000055163.7:p.Met1241Val
ENST00000414678.6:c.2287A>G	ENSP00000412835.2:p.Met763Val
NM_017519.2:c.3721A>G	NP_059989.2:p.Met1241Val
NM_020732.3:c.3760A>G	NP_065783.3:p.Met1254Val
XM_005267069.3:c.3880A>G	XP_005267126.2:p.Met1294Val
XM_011535984.1:c.2959A>G	XP_011534286.1:p.Met987Val
XM_011535985.1:c.2779A>G	XP_011534287.1:p.Met927Val
XM_011535986.1:c.2539A>G	XP_011534288.1:p.Met847Val
XM_011535987.1:c.2158A>G	XP_011534289.1:p.Met720Val
XM_011535988.1:c.1021A>G	XP_011534290.1:p.Met341Val
NM_001346813.1:c.3880A>G	NP_001333742.1:p.Met1294Val
NM_001363725.1:c.1630A>G	NP_001350654.1:p.Met544Val
XM_011535984.2:c.4090A>G	XP_011534286.2:p.Met1364Val
XM_011535988.3:c.1021A>G	XP_011534290.1:p.Met341Val
XM_017011103.2:c.3991A>G	XP_016866592.1:p.Met1331Val
XM_017011104.1:c.3961A>G	XP_016866593.1:p.Met1321Val
XM_017011105.2:c.3931A>G	XP_016866594.1:p.Met1311Val
XM_017011106.2:c.3802A>G	XP_016866595.1:p.Met1268Val
XM_017011107.2:c.3781A>G	XP_016866596.1:p.Met1261Val
XR_002956289.1:n.4173A>G
NM_001363725.2:c.1630A>G	NP_001350654.1:p.Met544Val
NM_001371656.1:c.4009A>G	NP_001358585.1:p.Met1337Val
NM_001374820.1:c.4009A>G	NP_001361749.1:p.Met1337Val
NM_001374828.1:c.4129A>G MANE Select	NP_001361757.1:p.Met1377Val
NM_017519.3:c.3970A>G	NP_059989.3:p.Met1324Val