Canonical Allele Identifier: CA366241672

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522176G>T (hg19) ; chr6:g.157201042G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201042G>T , CM000668.2:g.157201042G>T	GRCh38
NC_000006.11:g.157522176G>T , CM000668.1:g.157522176G>T	GRCh37
NC_000006.10:g.157563868G>T	NCBI36
NG_032093.1:g.428113G>T
NG_032093.2:g.428113G>T
NG_066624.1:g.430017G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4658G>T	ENSP00000055163.8:p.Gly1553Val
ENST00000414678.8:c.4727G>T	ENSP00000412835.3:p.Gly1576Val
ENST00000637015.2:c.4946G>T	ENSP00000489729.2:p.Gly1649Val
ENST00000346085.10:c.4697G>T	ENSP00000344546.5:p.Gly1566Val
ENST00000350026.10:c.4409G>T	ENSP00000055163.7:p.Gly1470Val
ENST00000414678.7:c.2975G>T	ENSP00000412835.2:p.Gly992Val
ENST00000635849.1:c.2138G>T	ENSP00000490948.1:p.Gly713Val
ENST00000635957.1:c.1769G>T	ENSP00000490385.1:p.Gly590Val
ENST00000636227.1:n.3280G>T
ENST00000636254.1:n.737G>T
ENST00000636930.2:c.4817G>T MANE Select	ENSP00000490491.2:p.Gly1606Val
ENST00000636940.1:n.2814G>T
ENST00000637015.1:c.2185G>T
ENST00000637568.1:c.2099G>T
ENST00000637741.1:n.1483G>T
ENST00000637810.1:c.2159G>T	ENSP00000489636.1:p.Gly720Val
ENST00000637904.1:c.2318G>T	ENSP00000490550.1:p.Gly773Val
ENST00000647938.1:c.4448G>T	ENSP00000498155.1:p.Gly1483Val
ENST00000346085.9:c.4448G>T	ENSP00000344546.4:p.Gly1483Val
ENST00000350026.9:c.4409G>T	ENSP00000055163.7:p.Gly1470Val
ENST00000414678.6:c.2975G>T	ENSP00000412835.2:p.Gly992Val
NM_017519.2:c.4409G>T	NP_059989.2:p.Gly1470Val
NM_020732.3:c.4448G>T	NP_065783.3:p.Gly1483Val
XM_005267069.3:c.4568G>T	XP_005267126.2:p.Gly1523Val
XM_011535984.1:c.3647G>T	XP_011534286.1:p.Gly1216Val
XM_011535985.1:c.3467G>T	XP_011534287.1:p.Gly1156Val
XM_011535986.1:c.3227G>T	XP_011534288.1:p.Gly1076Val
XM_011535987.1:c.2846G>T	XP_011534289.1:p.Gly949Val
XM_011535988.1:c.1709G>T	XP_011534290.1:p.Gly570Val
NM_001346813.1:c.4568G>T	NP_001333742.1:p.Gly1523Val
NM_001363725.1:c.2318G>T	NP_001350654.1:p.Gly773Val
XM_011535984.2:c.4778G>T	XP_011534286.2:p.Gly1593Val
XM_011535988.3:c.1709G>T	XP_011534290.1:p.Gly570Val
XM_017011103.2:c.4679G>T	XP_016866592.1:p.Gly1560Val
XM_017011104.1:c.4649G>T	XP_016866593.1:p.Gly1550Val
XM_017011105.2:c.4619G>T	XP_016866594.1:p.Gly1540Val
XM_017011106.2:c.4490G>T	XP_016866595.1:p.Gly1497Val
XM_017011107.2:c.4469G>T	XP_016866596.1:p.Gly1490Val
XR_002956289.1:n.4764G>T
NM_001363725.2:c.2318G>T	NP_001350654.1:p.Gly773Val
NM_001371656.1:c.4697G>T	NP_001358585.1:p.Gly1566Val
NM_001374820.1:c.4697G>T	NP_001361749.1:p.Gly1566Val
NM_001374828.1:c.4817G>T MANE Select	NP_001361757.1:p.Gly1606Val
NM_017519.3:c.4658G>T	NP_059989.3:p.Gly1553Val