Canonical Allele Identifier: CA366242325

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522380C>T (hg19) ; chr6:g.157201246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201246C>T , CM000668.2:g.157201246C>T	GRCh38
NC_000006.11:g.157522380C>T , CM000668.1:g.157522380C>T	GRCh37
NC_000006.10:g.157564072C>T	NCBI36
NG_032093.1:g.428317C>T
NG_032093.2:g.428317C>T
NG_066624.1:g.430221C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4862C>T	ENSP00000055163.8:p.Ser1621Phe
ENST00000414678.8:c.4931C>T	ENSP00000412835.3:p.Ser1644Phe
ENST00000637015.2:c.5150C>T	ENSP00000489729.2:p.Ser1717Phe
ENST00000346085.10:c.4901C>T	ENSP00000344546.5:p.Ser1634Phe
ENST00000350026.10:c.4613C>T	ENSP00000055163.7:p.Ser1538Phe
ENST00000414678.7:c.3179C>T	ENSP00000412835.2:p.Ser1060Phe
ENST00000635849.1:c.2342C>T	ENSP00000490948.1:p.Ser781Phe
ENST00000635957.1:c.1973C>T	ENSP00000490385.1:p.Ser658Phe
ENST00000636227.1:n.3484C>T
ENST00000636254.1:n.941C>T
ENST00000636930.2:c.5021C>T MANE Select	ENSP00000490491.2:p.Ser1674Phe
ENST00000636940.1:n.3018C>T
ENST00000637015.1:c.2389C>T
ENST00000637568.1:c.2303C>T
ENST00000637741.1:n.1687C>T
ENST00000637810.1:c.2363C>T	ENSP00000489636.1:p.Ser788Phe
ENST00000637904.1:c.2522C>T	ENSP00000490550.1:p.Ser841Phe
ENST00000647938.1:c.4652C>T	ENSP00000498155.1:p.Ser1551Phe
ENST00000346085.9:c.4652C>T	ENSP00000344546.4:p.Ser1551Phe
ENST00000350026.9:c.4613C>T	ENSP00000055163.7:p.Ser1538Phe
ENST00000414678.6:c.3179C>T	ENSP00000412835.2:p.Ser1060Phe
NM_017519.2:c.4613C>T	NP_059989.2:p.Ser1538Phe
NM_020732.3:c.4652C>T	NP_065783.3:p.Ser1551Phe
XM_005267069.3:c.4772C>T	XP_005267126.2:p.Ser1591Phe
XM_011535984.1:c.3851C>T	XP_011534286.1:p.Ser1284Phe
XM_011535985.1:c.3671C>T	XP_011534287.1:p.Ser1224Phe
XM_011535986.1:c.3431C>T	XP_011534288.1:p.Ser1144Phe
XM_011535987.1:c.3050C>T	XP_011534289.1:p.Ser1017Phe
XM_011535988.1:c.1913C>T	XP_011534290.1:p.Ser638Phe
NM_001346813.1:c.4772C>T	NP_001333742.1:p.Ser1591Phe
NM_001363725.1:c.2522C>T	NP_001350654.1:p.Ser841Phe
XM_011535984.2:c.4982C>T	XP_011534286.2:p.Ser1661Phe
XM_011535988.3:c.1913C>T	XP_011534290.1:p.Ser638Phe
XM_017011103.2:c.4883C>T	XP_016866592.1:p.Ser1628Phe
XM_017011104.1:c.4853C>T	XP_016866593.1:p.Ser1618Phe
XM_017011105.2:c.4823C>T	XP_016866594.1:p.Ser1608Phe
XM_017011106.2:c.4694C>T	XP_016866595.1:p.Ser1565Phe
XM_017011107.2:c.4673C>T	XP_016866596.1:p.Ser1558Phe
XR_002956289.1:n.4968C>T
NM_001363725.2:c.2522C>T	NP_001350654.1:p.Ser841Phe
NM_001371656.1:c.4901C>T	NP_001358585.1:p.Ser1634Phe
NM_001374820.1:c.4901C>T	NP_001361749.1:p.Ser1634Phe
NM_001374828.1:c.5021C>T MANE Select	NP_001361757.1:p.Ser1674Phe
NM_017519.3:c.4862C>T	NP_059989.3:p.Ser1621Phe