Canonical Allele Identifier: CA366239460

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554234947
• MyVariant Identifiers: chr6:g.157519949G>T (hg19) ; chr6:g.157198815G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198815G>T , CM000668.2:g.157198815G>T	GRCh38
NC_000006.11:g.157519949G>T , CM000668.1:g.157519949G>T	GRCh37
NC_000006.10:g.157561641G>T	NCBI36
NG_032093.1:g.425886G>T
NG_032093.2:g.425886G>T
NG_066624.1:g.427790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4228G>T	ENSP00000055163.8:p.Glu1410Ter
ENST00000414678.8:c.4297G>T	ENSP00000412835.3:p.Glu1433Ter
ENST00000637015.2:c.4516G>T	ENSP00000489729.2:p.Glu1506Ter
ENST00000346085.10:c.4267G>T	ENSP00000344546.5:p.Glu1423Ter
ENST00000350026.10:c.3979G>T	ENSP00000055163.7:p.Glu1327Ter
ENST00000414678.7:c.2545G>T	ENSP00000412835.2:p.Glu849Ter
ENST00000635849.1:c.1708G>T	ENSP00000490948.1:p.Glu570Ter
ENST00000635957.1:c.1339G>T	ENSP00000490385.1:p.Glu447Ter
ENST00000636227.1:n.2850G>T
ENST00000636254.1:n.307G>T
ENST00000636930.2:c.4387G>T MANE Select	ENSP00000490491.2:p.Glu1463Ter
ENST00000636940.1:n.2384G>T
ENST00000637015.1:c.1755G>T
ENST00000637568.1:c.1669G>T
ENST00000637741.1:n.1053G>T
ENST00000637810.1:c.1729G>T	ENSP00000489636.1:p.Glu577Ter
ENST00000637904.1:c.1888G>T	ENSP00000490550.1:p.Glu630Ter
ENST00000647938.1:c.4018G>T	ENSP00000498155.1:p.Glu1340Ter
ENST00000346085.9:c.4018G>T	ENSP00000344546.4:p.Glu1340Ter
ENST00000350026.9:c.3979G>T	ENSP00000055163.7:p.Glu1327Ter
ENST00000414678.6:c.2545G>T	ENSP00000412835.2:p.Glu849Ter
NM_017519.2:c.3979G>T	NP_059989.2:p.Glu1327Ter
NM_020732.3:c.4018G>T	NP_065783.3:p.Glu1340Ter
XM_005267069.3:c.4138G>T	XP_005267126.2:p.Glu1380Ter
XM_011535984.1:c.3217G>T	XP_011534286.1:p.Glu1073Ter
XM_011535985.1:c.3037G>T	XP_011534287.1:p.Glu1013Ter
XM_011535986.1:c.2797G>T	XP_011534288.1:p.Glu933Ter
XM_011535987.1:c.2416G>T	XP_011534289.1:p.Glu806Ter
XM_011535988.1:c.1279G>T	XP_011534290.1:p.Glu427Ter
NM_001346813.1:c.4138G>T	NP_001333742.1:p.Glu1380Ter
NM_001363725.1:c.1888G>T	NP_001350654.1:p.Glu630Ter
XM_011535984.2:c.4348G>T	XP_011534286.2:p.Glu1450Ter
XM_011535988.3:c.1279G>T	XP_011534290.1:p.Glu427Ter
XM_017011103.2:c.4249G>T	XP_016866592.1:p.Glu1417Ter
XM_017011104.1:c.4219G>T	XP_016866593.1:p.Glu1407Ter
XM_017011105.2:c.4189G>T	XP_016866594.1:p.Glu1397Ter
XM_017011106.2:c.4060G>T	XP_016866595.1:p.Glu1354Ter
XM_017011107.2:c.4039G>T	XP_016866596.1:p.Glu1347Ter
XR_002956289.1:n.4427-1890G>T
NM_001363725.2:c.1888G>T	NP_001350654.1:p.Glu630Ter
NM_001371656.1:c.4267G>T	NP_001358585.1:p.Glu1423Ter
NM_001374820.1:c.4267G>T	NP_001361749.1:p.Glu1423Ter
NM_001374828.1:c.4387G>T MANE Select	NP_001361757.1:p.Glu1463Ter
NM_017519.3:c.4228G>T	NP_059989.3:p.Glu1410Ter