Canonical Allele Identifier: CA366241678

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522178C>G (hg19) ; chr6:g.157201044C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201044C>G , CM000668.2:g.157201044C>G	GRCh38
NC_000006.11:g.157522178C>G , CM000668.1:g.157522178C>G	GRCh37
NC_000006.10:g.157563870C>G	NCBI36
NG_032093.1:g.428115C>G
NG_032093.2:g.428115C>G
NG_066624.1:g.430019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4660C>G	ENSP00000055163.8:p.Pro1554Ala
ENST00000414678.8:c.4729C>G	ENSP00000412835.3:p.Pro1577Ala
ENST00000637015.2:c.4948C>G	ENSP00000489729.2:p.Pro1650Ala
ENST00000346085.10:c.4699C>G	ENSP00000344546.5:p.Pro1567Ala
ENST00000350026.10:c.4411C>G	ENSP00000055163.7:p.Pro1471Ala
ENST00000414678.7:c.2977C>G	ENSP00000412835.2:p.Pro993Ala
ENST00000635849.1:c.2140C>G	ENSP00000490948.1:p.Pro714Ala
ENST00000635957.1:c.1771C>G	ENSP00000490385.1:p.Pro591Ala
ENST00000636227.1:n.3282C>G
ENST00000636254.1:n.739C>G
ENST00000636930.2:c.4819C>G MANE Select	ENSP00000490491.2:p.Pro1607Ala
ENST00000636940.1:n.2816C>G
ENST00000637015.1:c.2187C>G
ENST00000637568.1:c.2101C>G
ENST00000637741.1:n.1485C>G
ENST00000637810.1:c.2161C>G	ENSP00000489636.1:p.Pro721Ala
ENST00000637904.1:c.2320C>G	ENSP00000490550.1:p.Pro774Ala
ENST00000647938.1:c.4450C>G	ENSP00000498155.1:p.Pro1484Ala
ENST00000346085.9:c.4450C>G	ENSP00000344546.4:p.Pro1484Ala
ENST00000350026.9:c.4411C>G	ENSP00000055163.7:p.Pro1471Ala
ENST00000414678.6:c.2977C>G	ENSP00000412835.2:p.Pro993Ala
NM_017519.2:c.4411C>G	NP_059989.2:p.Pro1471Ala
NM_020732.3:c.4450C>G	NP_065783.3:p.Pro1484Ala
XM_005267069.3:c.4570C>G	XP_005267126.2:p.Pro1524Ala
XM_011535984.1:c.3649C>G	XP_011534286.1:p.Pro1217Ala
XM_011535985.1:c.3469C>G	XP_011534287.1:p.Pro1157Ala
XM_011535986.1:c.3229C>G	XP_011534288.1:p.Pro1077Ala
XM_011535987.1:c.2848C>G	XP_011534289.1:p.Pro950Ala
XM_011535988.1:c.1711C>G	XP_011534290.1:p.Pro571Ala
NM_001346813.1:c.4570C>G	NP_001333742.1:p.Pro1524Ala
NM_001363725.1:c.2320C>G	NP_001350654.1:p.Pro774Ala
XM_011535984.2:c.4780C>G	XP_011534286.2:p.Pro1594Ala
XM_011535988.3:c.1711C>G	XP_011534290.1:p.Pro571Ala
XM_017011103.2:c.4681C>G	XP_016866592.1:p.Pro1561Ala
XM_017011104.1:c.4651C>G	XP_016866593.1:p.Pro1551Ala
XM_017011105.2:c.4621C>G	XP_016866594.1:p.Pro1541Ala
XM_017011106.2:c.4492C>G	XP_016866595.1:p.Pro1498Ala
XM_017011107.2:c.4471C>G	XP_016866596.1:p.Pro1491Ala
XR_002956289.1:n.4766C>G
NM_001363725.2:c.2320C>G	NP_001350654.1:p.Pro774Ala
NM_001371656.1:c.4699C>G	NP_001358585.1:p.Pro1567Ala
NM_001374820.1:c.4699C>G	NP_001361749.1:p.Pro1567Ala
NM_001374828.1:c.4819C>G MANE Select	NP_001361757.1:p.Pro1607Ala
NM_017519.3:c.4660C>G	NP_059989.3:p.Pro1554Ala