Canonical Allele Identifier: CA366382827

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2845792
• ClinVar RCV Id: RCV003687588
• gnomAD v4: 6-156778701-C-T
• MyVariant Identifiers: chr6:g.157099835C>T (hg19) ; chr6:g.156778701C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156778701C>T , CM000668.2:g.156778701C>T	GRCh38
NC_000006.11:g.157099835C>T , CM000668.1:g.157099835C>T	GRCh37
NC_000006.10:g.157141527C>T	NCBI36
NG_032093.1:g.5772C>T
NG_032093.2:g.5772C>T
NG_066624.1:g.7676C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.1021C>T	ENSP00000055163.8:p.Gln341Ter
ENST00000414678.8:c.1021C>T	ENSP00000412835.3:p.Gln341Ter
ENST00000637015.2:c.1021C>T	ENSP00000489729.2:p.Gln341Ter
ENST00000346085.10:c.1021C>T	ENSP00000344546.5:p.Gln341Ter
ENST00000350026.10:c.772C>T	ENSP00000055163.7:p.Gln258Ter
ENST00000636930.2:c.1021C>T MANE Select	ENSP00000490491.2:p.Gln341Ter
ENST00000647938.1:c.772C>T	ENSP00000498155.1:p.Gln258Ter
ENST00000674298.1:c.761C>T
ENST00000346085.9:c.772C>T	ENSP00000344546.4:p.Gln258Ter
ENST00000350026.9:c.772C>T	ENSP00000055163.7:p.Gln258Ter
NM_017519.2:c.772C>T	NP_059989.2:p.Gln258Ter
NM_020732.3:c.772C>T	NP_065783.3:p.Gln258Ter
XM_005267069.3:c.772C>T	XP_005267126.2:p.Gln258Ter
NM_001346813.1:c.772C>T	NP_001333742.1:p.Gln258Ter
XM_011535984.2:c.772C>T	XP_011534286.2:p.Gln258Ter
XM_017011103.2:c.772C>T	XP_016866592.1:p.Gln258Ter
XM_017011104.1:c.772C>T	XP_016866593.1:p.Gln258Ter
XM_017011105.2:c.772C>T	XP_016866594.1:p.Gln258Ter
XM_017011106.2:c.772C>T	XP_016866595.1:p.Gln258Ter
XM_017011107.2:c.772C>T	XP_016866596.1:p.Gln258Ter
XR_002956289.1:n.855C>T
NM_001371656.1:c.1021C>T	NP_001358585.1:p.Gln341Ter
NM_001374820.1:c.1021C>T	NP_001361749.1:p.Gln341Ter
NM_001374828.1:c.1021C>T MANE Select	NP_001361757.1:p.Gln341Ter
NM_017519.3:c.1021C>T	NP_059989.3:p.Gln341Ter