Canonical Allele Identifier: CA366242432

Gene: ARID1B

Linked Data

• dbSNP Id: rs1284190943
• gnomAD v3: 6-157201297-C-G
• gnomAD v4: 6-157201297-C-G
• MyVariant Identifiers: chr6:g.157522431C>G (hg19) ; chr6:g.157201297C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201297C>G , CM000668.2:g.157201297C>G	GRCh38
NC_000006.11:g.157522431C>G , CM000668.1:g.157522431C>G	GRCh37
NC_000006.10:g.157564123C>G	NCBI36
NG_032093.1:g.428368C>G
NG_032093.2:g.428368C>G
NG_066624.1:g.430272C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4913C>G	ENSP00000055163.8:p.Ser1638Cys
ENST00000414678.8:c.4982C>G	ENSP00000412835.3:p.Ser1661Cys
ENST00000637015.2:c.5201C>G	ENSP00000489729.2:p.Ser1734Cys
ENST00000346085.10:c.4952C>G	ENSP00000344546.5:p.Ser1651Cys
ENST00000350026.10:c.4664C>G	ENSP00000055163.7:p.Ser1555Cys
ENST00000414678.7:c.3230C>G	ENSP00000412835.2:p.Ser1077Cys
ENST00000635849.1:c.2393C>G	ENSP00000490948.1:p.Ser798Cys
ENST00000635957.1:c.2024C>G	ENSP00000490385.1:p.Ser675Cys
ENST00000636227.1:n.3535C>G
ENST00000636254.1:n.992C>G
ENST00000636930.2:c.5072C>G MANE Select	ENSP00000490491.2:p.Ser1691Cys
ENST00000636940.1:n.3069C>G
ENST00000637015.1:c.2440C>G
ENST00000637568.1:c.2354C>G
ENST00000637741.1:n.1738C>G
ENST00000637810.1:c.2414C>G	ENSP00000489636.1:p.Ser805Cys
ENST00000637904.1:c.2573C>G	ENSP00000490550.1:p.Ser858Cys
ENST00000647938.1:c.4703C>G	ENSP00000498155.1:p.Ser1568Cys
ENST00000346085.9:c.4703C>G	ENSP00000344546.4:p.Ser1568Cys
ENST00000350026.9:c.4664C>G	ENSP00000055163.7:p.Ser1555Cys
ENST00000414678.6:c.3230C>G	ENSP00000412835.2:p.Ser1077Cys
NM_017519.2:c.4664C>G	NP_059989.2:p.Ser1555Cys
NM_020732.3:c.4703C>G	NP_065783.3:p.Ser1568Cys
XM_005267069.3:c.4823C>G	XP_005267126.2:p.Ser1608Cys
XM_011535984.1:c.3902C>G	XP_011534286.1:p.Ser1301Cys
XM_011535985.1:c.3722C>G	XP_011534287.1:p.Ser1241Cys
XM_011535986.1:c.3482C>G	XP_011534288.1:p.Ser1161Cys
XM_011535987.1:c.3101C>G	XP_011534289.1:p.Ser1034Cys
XM_011535988.1:c.1964C>G	XP_011534290.1:p.Ser655Cys
NM_001346813.1:c.4823C>G	NP_001333742.1:p.Ser1608Cys
NM_001363725.1:c.2573C>G	NP_001350654.1:p.Ser858Cys
XM_011535984.2:c.5033C>G	XP_011534286.2:p.Ser1678Cys
XM_011535988.3:c.1964C>G	XP_011534290.1:p.Ser655Cys
XM_017011103.2:c.4934C>G	XP_016866592.1:p.Ser1645Cys
XM_017011104.1:c.4904C>G	XP_016866593.1:p.Ser1635Cys
XM_017011105.2:c.4874C>G	XP_016866594.1:p.Ser1625Cys
XM_017011106.2:c.4745C>G	XP_016866595.1:p.Ser1582Cys
XM_017011107.2:c.4724C>G	XP_016866596.1:p.Ser1575Cys
XR_002956289.1:n.5019C>G
NM_001363725.2:c.2573C>G	NP_001350654.1:p.Ser858Cys
NM_001371656.1:c.4952C>G	NP_001358585.1:p.Ser1651Cys
NM_001374820.1:c.4952C>G	NP_001361749.1:p.Ser1651Cys
NM_001374828.1:c.5072C>G MANE Select	NP_001361757.1:p.Ser1691Cys
NM_017519.3:c.4913C>G	NP_059989.3:p.Ser1638Cys