Canonical Allele Identifier: CA366246217

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157206392-G-T
• MyVariant Identifiers: chr6:g.157527526G>T (hg19) ; chr6:g.157206392G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206392G>T , CM000668.2:g.157206392G>T	GRCh38
NC_000006.11:g.157527526G>T , CM000668.1:g.157527526G>T	GRCh37
NC_000006.10:g.157569218G>T	NCBI36
NG_032093.1:g.433463G>T
NG_032093.2:g.433463G>T
NG_066624.1:g.435367G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.5461G>T	ENSP00000055163.8:p.Asp1821Tyr
ENST00000414678.8:c.5530G>T	ENSP00000412835.3:p.Asp1844Tyr
ENST00000637015.2:c.5749G>T	ENSP00000489729.2:p.Asp1917Tyr
ENST00000346085.10:c.5500G>T	ENSP00000344546.5:p.Asp1834Tyr
ENST00000350026.10:c.5212G>T	ENSP00000055163.7:p.Asp1738Tyr
ENST00000414678.7:c.3778G>T	ENSP00000412835.2:p.Asp1260Tyr
ENST00000635849.1:c.2941G>T	ENSP00000490948.1:p.Asp981Tyr
ENST00000635957.1:c.2572G>T	ENSP00000490385.1:p.Asp858Tyr
ENST00000636227.1:n.4083G>T
ENST00000636254.1:n.1540G>T
ENST00000636930.2:c.5620G>T MANE Select	ENSP00000490491.2:p.Asp1874Tyr
ENST00000636940.1:n.3617G>T
ENST00000637015.1:c.2988G>T
ENST00000637568.1:c.2902G>T
ENST00000637741.1:n.2286G>T
ENST00000637810.1:c.2962G>T	ENSP00000489636.1:p.Asp988Tyr
ENST00000637904.1:c.3121G>T	ENSP00000490550.1:p.Asp1041Tyr
ENST00000637933.1:n.2735G>T
ENST00000647938.1:c.5251G>T	ENSP00000498155.1:p.Asp1751Tyr
ENST00000346085.9:c.5251G>T	ENSP00000344546.4:p.Asp1751Tyr
ENST00000350026.9:c.5212G>T	ENSP00000055163.7:p.Asp1738Tyr
ENST00000414678.6:c.3778G>T	ENSP00000412835.2:p.Asp1260Tyr
NM_017519.2:c.5212G>T	NP_059989.2:p.Asp1738Tyr
NM_020732.3:c.5251G>T	NP_065783.3:p.Asp1751Tyr
XM_005267069.3:c.5371G>T	XP_005267126.2:p.Asp1791Tyr
XM_011535984.1:c.4450G>T	XP_011534286.1:p.Asp1484Tyr
XM_011535985.1:c.4270G>T	XP_011534287.1:p.Asp1424Tyr
XM_011535986.1:c.4030G>T	XP_011534288.1:p.Asp1344Tyr
XM_011535987.1:c.3649G>T	XP_011534289.1:p.Asp1217Tyr
XM_011535988.1:c.2512G>T	XP_011534290.1:p.Asp838Tyr
NM_001346813.1:c.5371G>T	NP_001333742.1:p.Asp1791Tyr
NM_001363725.1:c.3121G>T	NP_001350654.1:p.Asp1041Tyr
XM_011535984.2:c.5581G>T	XP_011534286.2:p.Asp1861Tyr
XM_011535988.3:c.2512G>T	XP_011534290.1:p.Asp838Tyr
XM_017011103.2:c.5482G>T	XP_016866592.1:p.Asp1828Tyr
XM_017011104.1:c.5452G>T	XP_016866593.1:p.Asp1818Tyr
XM_017011105.2:c.5422G>T	XP_016866594.1:p.Asp1808Tyr
XM_017011106.2:c.5293G>T	XP_016866595.1:p.Asp1765Tyr
XM_017011107.2:c.5272G>T	XP_016866596.1:p.Asp1758Tyr
XR_002956289.1:n.5567G>T
NM_001363725.2:c.3121G>T	NP_001350654.1:p.Asp1041Tyr
NM_001371656.1:c.5500G>T	NP_001358585.1:p.Asp1834Tyr
NM_001374820.1:c.5500G>T	NP_001361749.1:p.Asp1834Tyr
NM_001374828.1:c.5620G>T MANE Select	NP_001361757.1:p.Asp1874Tyr
NM_017519.3:c.5461G>T	NP_059989.3:p.Asp1821Tyr