Canonical Allele Identifier: CA366235080

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511219C>G (hg19) ; chr6:g.157190085C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190085C>G , CM000668.2:g.157190085C>G	GRCh38
NC_000006.11:g.157511219C>G , CM000668.1:g.157511219C>G	GRCh37
NC_000006.10:g.157552911C>G	NCBI36
NG_032093.1:g.417156C>G
NG_032093.2:g.417156C>G
NG_066624.1:g.419060C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3947C>G	ENSP00000055163.8:p.Ser1316Ter
ENST00000414678.8:c.4016C>G	ENSP00000412835.3:p.Ser1339Ter
ENST00000637015.2:c.4235C>G	ENSP00000489729.2:p.Ser1412Ter
ENST00000346085.10:c.3986C>G	ENSP00000344546.5:p.Ser1329Ter
ENST00000350026.10:c.3698C>G	ENSP00000055163.7:p.Ser1233Ter
ENST00000414678.7:c.2264C>G	ENSP00000412835.2:p.Ser755Ter
ENST00000635849.1:c.1427C>G	ENSP00000490948.1:p.Ser476Ter
ENST00000635957.1:c.1058C>G	ENSP00000490385.1:p.Ser353Ter
ENST00000636930.2:c.4106C>G MANE Select	ENSP00000490491.2:p.Ser1369Ter
ENST00000636940.1:n.2103C>G
ENST00000637015.1:c.1474C>G
ENST00000637568.1:c.1388C>G
ENST00000637741.1:n.772C>G
ENST00000637810.1:c.1448C>G	ENSP00000489636.1:p.Ser483Ter
ENST00000637904.1:c.1607C>G	ENSP00000490550.1:p.Ser536Ter
ENST00000647938.1:c.3737C>G	ENSP00000498155.1:p.Ser1246Ter
ENST00000346085.9:c.3737C>G	ENSP00000344546.4:p.Ser1246Ter
ENST00000350026.9:c.3698C>G	ENSP00000055163.7:p.Ser1233Ter
ENST00000414678.6:c.2264C>G	ENSP00000412835.2:p.Ser755Ter
NM_017519.2:c.3698C>G	NP_059989.2:p.Ser1233Ter
NM_020732.3:c.3737C>G	NP_065783.3:p.Ser1246Ter
XM_005267069.3:c.3857C>G	XP_005267126.2:p.Ser1286Ter
XM_011535984.1:c.2936C>G	XP_011534286.1:p.Ser979Ter
XM_011535985.1:c.2756C>G	XP_011534287.1:p.Ser919Ter
XM_011535986.1:c.2516C>G	XP_011534288.1:p.Ser839Ter
XM_011535987.1:c.2135C>G	XP_011534289.1:p.Ser712Ter
XM_011535988.1:c.998C>G	XP_011534290.1:p.Ser333Ter
NM_001346813.1:c.3857C>G	NP_001333742.1:p.Ser1286Ter
NM_001363725.1:c.1607C>G	NP_001350654.1:p.Ser536Ter
XM_011535984.2:c.4067C>G	XP_011534286.2:p.Ser1356Ter
XM_011535988.3:c.998C>G	XP_011534290.1:p.Ser333Ter
XM_017011103.2:c.3968C>G	XP_016866592.1:p.Ser1323Ter
XM_017011104.1:c.3938C>G	XP_016866593.1:p.Ser1313Ter
XM_017011105.2:c.3908C>G	XP_016866594.1:p.Ser1303Ter
XM_017011106.2:c.3779C>G	XP_016866595.1:p.Ser1260Ter
XM_017011107.2:c.3758C>G	XP_016866596.1:p.Ser1253Ter
XR_002956289.1:n.4150C>G
NM_001363725.2:c.1607C>G	NP_001350654.1:p.Ser536Ter
NM_001371656.1:c.3986C>G	NP_001358585.1:p.Ser1329Ter
NM_001374820.1:c.3986C>G	NP_001361749.1:p.Ser1329Ter
NM_001374828.1:c.4106C>G MANE Select	NP_001361757.1:p.Ser1369Ter
NM_017519.3:c.3947C>G	NP_059989.3:p.Ser1316Ter