Canonical Allele Identifier: CA4067530

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1924934
• ClinVar RCV Id: RCV002625864
• dbSNP Id: rs376071880
• ExAC: 6:157511252 A / G
• gnomAD v2: 6-157511252-A-G
• gnomAD v3: 6-157190118-A-G
• gnomAD v4: 6-157190118-A-G
• MyVariant Identifiers: chr6:g.157511252A>G (hg19) ; chr6:g.157190118A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190118A>G , CM000668.2:g.157190118A>G	GRCh38
NC_000006.11:g.157511252A>G , CM000668.1:g.157511252A>G	GRCh37
NC_000006.10:g.157552944A>G	NCBI36
NG_032093.1:g.417189A>G
NG_032093.2:g.417189A>G
NG_066624.1:g.419093A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3980A>G	ENSP00000055163.8:p.Asn1327Ser
ENST00000414678.8:c.4049A>G	ENSP00000412835.3:p.Asn1350Ser
ENST00000637015.2:c.4268A>G	ENSP00000489729.2:p.Asn1423Ser
ENST00000346085.10:c.4019A>G	ENSP00000344546.5:p.Asn1340Ser
ENST00000350026.10:c.3731A>G	ENSP00000055163.7:p.Asn1244Ser
ENST00000414678.7:c.2297A>G	ENSP00000412835.2:p.Asn766Ser
ENST00000635849.1:c.1460A>G	ENSP00000490948.1:p.Asn487Ser
ENST00000635957.1:c.1091A>G	ENSP00000490385.1:p.Asn364Ser
ENST00000636930.2:c.4139A>G MANE Select	ENSP00000490491.2:p.Asn1380Ser
ENST00000636940.1:n.2136A>G
ENST00000637015.1:c.1507A>G
ENST00000637568.1:c.1421A>G
ENST00000637741.1:n.805A>G
ENST00000637810.1:c.1481A>G	ENSP00000489636.1:p.Asn494Ser
ENST00000637904.1:c.1640A>G	ENSP00000490550.1:p.Asn547Ser
ENST00000647938.1:c.3770A>G	ENSP00000498155.1:p.Asn1257Ser
ENST00000346085.9:c.3770A>G	ENSP00000344546.4:p.Asn1257Ser
ENST00000350026.9:c.3731A>G	ENSP00000055163.7:p.Asn1244Ser
ENST00000414678.6:c.2297A>G	ENSP00000412835.2:p.Asn766Ser
NM_017519.2:c.3731A>G	NP_059989.2:p.Asn1244Ser
NM_020732.3:c.3770A>G	NP_065783.3:p.Asn1257Ser
XM_005267069.3:c.3890A>G	XP_005267126.2:p.Asn1297Ser
XM_011535984.1:c.2969A>G	XP_011534286.1:p.Asn990Ser
XM_011535985.1:c.2789A>G	XP_011534287.1:p.Asn930Ser
XM_011535986.1:c.2549A>G	XP_011534288.1:p.Asn850Ser
XM_011535987.1:c.2168A>G	XP_011534289.1:p.Asn723Ser
XM_011535988.1:c.1031A>G	XP_011534290.1:p.Asn344Ser
NM_001346813.1:c.3890A>G	NP_001333742.1:p.Asn1297Ser
NM_001363725.1:c.1640A>G	NP_001350654.1:p.Asn547Ser
XM_011535984.2:c.4100A>G	XP_011534286.2:p.Asn1367Ser
XM_011535988.3:c.1031A>G	XP_011534290.1:p.Asn344Ser
XM_017011103.2:c.4001A>G	XP_016866592.1:p.Asn1334Ser
XM_017011104.1:c.3971A>G	XP_016866593.1:p.Asn1324Ser
XM_017011105.2:c.3941A>G	XP_016866594.1:p.Asn1314Ser
XM_017011106.2:c.3812A>G	XP_016866595.1:p.Asn1271Ser
XM_017011107.2:c.3791A>G	XP_016866596.1:p.Asn1264Ser
XR_002956289.1:n.4183A>G
NM_001363725.2:c.1640A>G	NP_001350654.1:p.Asn547Ser
NM_001371656.1:c.4019A>G	NP_001358585.1:p.Asn1340Ser
NM_001374820.1:c.4019A>G	NP_001361749.1:p.Asn1340Ser
NM_001374828.1:c.4139A>G MANE Select	NP_001361757.1:p.Asn1380Ser
NM_017519.3:c.3980A>G	NP_059989.3:p.Asn1327Ser