Canonical Allele Identifier: CA16043663

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 374256
• ClinVar RCV Id: RCV000414923 ; RCV001533081
• dbSNP Id: rs1057518648
• MyVariant Identifiers: chr6:g.157099080G>A (hg19) ; chr6:g.156777946G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156777946G>A , CM000668.2:g.156777946G>A	GRCh38
NC_000006.11:g.157099080G>A , CM000668.1:g.157099080G>A	GRCh37
NC_000006.10:g.157140772G>A	NCBI36
NG_032093.1:g.5017G>A
NG_032093.2:g.5017G>A
NG_066624.1:g.6921G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.266G>A	ENSP00000055163.8:p.Gly89Asp
ENST00000414678.8:c.266G>A	ENSP00000412835.3:p.Gly89Asp
ENST00000637015.2:c.266G>A	ENSP00000489729.2:p.Gly89Asp
ENST00000346085.10:c.266G>A	ENSP00000344546.5:p.Gly89Asp
ENST00000350026.10:c.17G>A	ENSP00000055163.7:p.Gly6Asp
ENST00000636930.2:c.266G>A MANE Select	ENSP00000490491.2:p.Gly89Asp
ENST00000647938.1:c.17G>A	ENSP00000498155.1:p.Gly6Asp
ENST00000674298.1:c.6G>A
ENST00000346085.9:c.17G>A	ENSP00000344546.4:p.Gly6Asp
ENST00000350026.9:c.17G>A	ENSP00000055163.7:p.Gly6Asp
NM_017519.2:c.17G>A	NP_059989.2:p.Gly6Asp
NM_020732.3:c.17G>A	NP_065783.3:p.Gly6Asp
XM_005267069.3:c.17G>A	XP_005267126.2:p.Gly6Asp
XR_943148.1:n.177+300C>T
NM_001346813.1:c.17G>A	NP_001333742.1:p.Gly6Asp
XM_011535984.2:c.17G>A	XP_011534286.2:p.Gly6Asp
XM_017011103.2:c.17G>A	XP_016866592.1:p.Gly6Asp
XM_017011104.1:c.17G>A	XP_016866593.1:p.Gly6Asp
XM_017011105.2:c.17G>A	XP_016866594.1:p.Gly6Asp
XM_017011106.2:c.17G>A	XP_016866595.1:p.Gly6Asp
XM_017011107.2:c.17G>A	XP_016866596.1:p.Gly6Asp
XR_002956289.1:n.100G>A
NM_001371656.1:c.266G>A	NP_001358585.1:p.Gly89Asp
NM_001374820.1:c.266G>A	NP_001361749.1:p.Gly89Asp
NM_001374828.1:c.266G>A MANE Select	NP_001361757.1:p.Gly89Asp
NM_017519.3:c.266G>A	NP_059989.3:p.Gly89Asp
NR_163974.1:n.273+300C>T