Canonical Allele Identifier: CA366239680

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157198846-G-T
• MyVariant Identifiers: chr6:g.157519980G>T (hg19) ; chr6:g.157198846G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198846G>T , CM000668.2:g.157198846G>T	GRCh38
NC_000006.11:g.157519980G>T , CM000668.1:g.157519980G>T	GRCh37
NC_000006.10:g.157561672G>T	NCBI36
NG_032093.1:g.425917G>T
NG_032093.2:g.425917G>T
NG_066624.1:g.427821G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4259G>T	ENSP00000055163.8:p.Gly1420Val
ENST00000414678.8:c.4328G>T	ENSP00000412835.3:p.Gly1443Val
ENST00000637015.2:c.4547G>T	ENSP00000489729.2:p.Gly1516Val
ENST00000346085.10:c.4298G>T	ENSP00000344546.5:p.Gly1433Val
ENST00000350026.10:c.4010G>T	ENSP00000055163.7:p.Gly1337Val
ENST00000414678.7:c.2576G>T	ENSP00000412835.2:p.Gly859Val
ENST00000635849.1:c.1739G>T	ENSP00000490948.1:p.Gly580Val
ENST00000635957.1:c.1370G>T	ENSP00000490385.1:p.Gly457Val
ENST00000636227.1:n.2881G>T
ENST00000636254.1:n.338G>T
ENST00000636930.2:c.4418G>T MANE Select	ENSP00000490491.2:p.Gly1473Val
ENST00000636940.1:n.2415G>T
ENST00000637015.1:c.1786G>T
ENST00000637568.1:c.1700G>T
ENST00000637741.1:n.1084G>T
ENST00000637810.1:c.1760G>T	ENSP00000489636.1:p.Gly587Val
ENST00000637904.1:c.1919G>T	ENSP00000490550.1:p.Gly640Val
ENST00000647938.1:c.4049G>T	ENSP00000498155.1:p.Gly1350Val
ENST00000346085.9:c.4049G>T	ENSP00000344546.4:p.Gly1350Val
ENST00000350026.9:c.4010G>T	ENSP00000055163.7:p.Gly1337Val
ENST00000414678.6:c.2576G>T	ENSP00000412835.2:p.Gly859Val
NM_017519.2:c.4010G>T	NP_059989.2:p.Gly1337Val
NM_020732.3:c.4049G>T	NP_065783.3:p.Gly1350Val
XM_005267069.3:c.4169G>T	XP_005267126.2:p.Gly1390Val
XM_011535984.1:c.3248G>T	XP_011534286.1:p.Gly1083Val
XM_011535985.1:c.3068G>T	XP_011534287.1:p.Gly1023Val
XM_011535986.1:c.2828G>T	XP_011534288.1:p.Gly943Val
XM_011535987.1:c.2447G>T	XP_011534289.1:p.Gly816Val
XM_011535988.1:c.1310G>T	XP_011534290.1:p.Gly437Val
NM_001346813.1:c.4169G>T	NP_001333742.1:p.Gly1390Val
NM_001363725.1:c.1919G>T	NP_001350654.1:p.Gly640Val
XM_011535984.2:c.4379G>T	XP_011534286.2:p.Gly1460Val
XM_011535988.3:c.1310G>T	XP_011534290.1:p.Gly437Val
XM_017011103.2:c.4280G>T	XP_016866592.1:p.Gly1427Val
XM_017011104.1:c.4250G>T	XP_016866593.1:p.Gly1417Val
XM_017011105.2:c.4220G>T	XP_016866594.1:p.Gly1407Val
XM_017011106.2:c.4091G>T	XP_016866595.1:p.Gly1364Val
XM_017011107.2:c.4070G>T	XP_016866596.1:p.Gly1357Val
XR_002956289.1:n.4427-1859G>T
NM_001363725.2:c.1919G>T	NP_001350654.1:p.Gly640Val
NM_001371656.1:c.4298G>T	NP_001358585.1:p.Gly1433Val
NM_001374820.1:c.4298G>T	NP_001361749.1:p.Gly1433Val
NM_001374828.1:c.4418G>T MANE Select	NP_001361757.1:p.Gly1473Val
NM_017519.3:c.4259G>T	NP_059989.3:p.Gly1420Val