Canonical Allele Identifier: CA209558

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 210272
• ClinVar RCV Id: RCV000195009 ; RCV000513748 ; RCV001807122 ; RCV002415818 ; RCV003937683
• dbSNP Id: rs776745618
• ExAC: 6:157099260 A / G
• gnomAD v2: 6-157099260-A-G
• gnomAD v3: 6-156778126-A-G
• gnomAD v4: 6-156778126-A-G
• MyVariant Identifiers: chr6:g.157099260A>G (hg19) ; chr6:g.156778126A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156778126A>G , CM000668.2:g.156778126A>G	GRCh38
NC_000006.11:g.157099260A>G , CM000668.1:g.157099260A>G	GRCh37
NC_000006.10:g.157140952A>G	NCBI36
NG_032093.1:g.5197A>G
NG_032093.2:g.5197A>G
NG_066624.1:g.7101A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.446A>G	ENSP00000055163.8:p.Asn149Ser
ENST00000414678.8:c.446A>G	ENSP00000412835.3:p.Asn149Ser
ENST00000637015.2:c.446A>G	ENSP00000489729.2:p.Asn149Ser
ENST00000346085.10:c.446A>G	ENSP00000344546.5:p.Asn149Ser
ENST00000350026.10:c.197A>G	ENSP00000055163.7:p.Asn66Ser
ENST00000636930.2:c.446A>G MANE Select	ENSP00000490491.2:p.Asn149Ser
ENST00000647938.1:c.197A>G	ENSP00000498155.1:p.Asn66Ser
ENST00000674298.1:c.186A>G
ENST00000346085.9:c.197A>G	ENSP00000344546.4:p.Asn66Ser
ENST00000350026.9:c.197A>G	ENSP00000055163.7:p.Asn66Ser
NM_017519.2:c.197A>G	NP_059989.2:p.Asn66Ser
NM_020732.3:c.197A>G	NP_065783.3:p.Asn66Ser
XM_005267069.3:c.197A>G	XP_005267126.2:p.Asn66Ser
XR_943148.1:n.177+120T>C
NM_001346813.1:c.197A>G	NP_001333742.1:p.Asn66Ser
XM_011535984.2:c.197A>G	XP_011534286.2:p.Asn66Ser
XM_017011103.2:c.197A>G	XP_016866592.1:p.Asn66Ser
XM_017011104.1:c.197A>G	XP_016866593.1:p.Asn66Ser
XM_017011105.2:c.197A>G	XP_016866594.1:p.Asn66Ser
XM_017011106.2:c.197A>G	XP_016866595.1:p.Asn66Ser
XM_017011107.2:c.197A>G	XP_016866596.1:p.Asn66Ser
XR_002956289.1:n.280A>G
NM_001371656.1:c.446A>G	NP_001358585.1:p.Asn149Ser
NM_001374820.1:c.446A>G	NP_001361749.1:p.Asn149Ser
NM_001374828.1:c.446A>G MANE Select	NP_001361757.1:p.Asn149Ser
NM_017519.3:c.446A>G	NP_059989.3:p.Asn149Ser
NR_163974.1:n.273+120T>C