Canonical Allele Identifier: CA366242458

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522442T>G (hg19) ; chr6:g.157201308T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201308T>G , CM000668.2:g.157201308T>G	GRCh38
NC_000006.11:g.157522442T>G , CM000668.1:g.157522442T>G	GRCh37
NC_000006.10:g.157564134T>G	NCBI36
NG_032093.1:g.428379T>G
NG_032093.2:g.428379T>G
NG_066624.1:g.430283T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4924T>G	ENSP00000055163.8:p.Ser1642Ala
ENST00000414678.8:c.4993T>G	ENSP00000412835.3:p.Ser1665Ala
ENST00000637015.2:c.5212T>G	ENSP00000489729.2:p.Ser1738Ala
ENST00000346085.10:c.4963T>G	ENSP00000344546.5:p.Ser1655Ala
ENST00000350026.10:c.4675T>G	ENSP00000055163.7:p.Ser1559Ala
ENST00000414678.7:c.3241T>G	ENSP00000412835.2:p.Ser1081Ala
ENST00000635849.1:c.2404T>G	ENSP00000490948.1:p.Ser802Ala
ENST00000635957.1:c.2035T>G	ENSP00000490385.1:p.Ser679Ala
ENST00000636227.1:n.3546T>G
ENST00000636254.1:n.1003T>G
ENST00000636930.2:c.5083T>G MANE Select	ENSP00000490491.2:p.Ser1695Ala
ENST00000636940.1:n.3080T>G
ENST00000637015.1:c.2451T>G
ENST00000637568.1:c.2365T>G
ENST00000637741.1:n.1749T>G
ENST00000637810.1:c.2425T>G	ENSP00000489636.1:p.Ser809Ala
ENST00000637904.1:c.2584T>G	ENSP00000490550.1:p.Ser862Ala
ENST00000647938.1:c.4714T>G	ENSP00000498155.1:p.Ser1572Ala
ENST00000346085.9:c.4714T>G	ENSP00000344546.4:p.Ser1572Ala
ENST00000350026.9:c.4675T>G	ENSP00000055163.7:p.Ser1559Ala
ENST00000414678.6:c.3241T>G	ENSP00000412835.2:p.Ser1081Ala
NM_017519.2:c.4675T>G	NP_059989.2:p.Ser1559Ala
NM_020732.3:c.4714T>G	NP_065783.3:p.Ser1572Ala
XM_005267069.3:c.4834T>G	XP_005267126.2:p.Ser1612Ala
XM_011535984.1:c.3913T>G	XP_011534286.1:p.Ser1305Ala
XM_011535985.1:c.3733T>G	XP_011534287.1:p.Ser1245Ala
XM_011535986.1:c.3493T>G	XP_011534288.1:p.Ser1165Ala
XM_011535987.1:c.3112T>G	XP_011534289.1:p.Ser1038Ala
XM_011535988.1:c.1975T>G	XP_011534290.1:p.Ser659Ala
NM_001346813.1:c.4834T>G	NP_001333742.1:p.Ser1612Ala
NM_001363725.1:c.2584T>G	NP_001350654.1:p.Ser862Ala
XM_011535984.2:c.5044T>G	XP_011534286.2:p.Ser1682Ala
XM_011535988.3:c.1975T>G	XP_011534290.1:p.Ser659Ala
XM_017011103.2:c.4945T>G	XP_016866592.1:p.Ser1649Ala
XM_017011104.1:c.4915T>G	XP_016866593.1:p.Ser1639Ala
XM_017011105.2:c.4885T>G	XP_016866594.1:p.Ser1629Ala
XM_017011106.2:c.4756T>G	XP_016866595.1:p.Ser1586Ala
XM_017011107.2:c.4735T>G	XP_016866596.1:p.Ser1579Ala
XR_002956289.1:n.5030T>G
NM_001363725.2:c.2584T>G	NP_001350654.1:p.Ser862Ala
NM_001371656.1:c.4963T>G	NP_001358585.1:p.Ser1655Ala
NM_001374820.1:c.4963T>G	NP_001361749.1:p.Ser1655Ala
NM_001374828.1:c.5083T>G MANE Select	NP_001361757.1:p.Ser1695Ala
NM_017519.3:c.4924T>G	NP_059989.3:p.Ser1642Ala