Canonical Allele Identifier: CA366239676

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793919837
• MyVariant Identifiers: chr6:g.157519980G>C (hg19) ; chr6:g.157198846G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4259G>C	ENSP00000055163.8:p.Gly1420Ala
ENST00000414678.8:c.4328G>C	ENSP00000412835.3:p.Gly1443Ala
ENST00000637015.2:c.4547G>C	ENSP00000489729.2:p.Gly1516Ala
ENST00000346085.10:c.4298G>C	ENSP00000344546.5:p.Gly1433Ala
ENST00000350026.10:c.4010G>C	ENSP00000055163.7:p.Gly1337Ala
ENST00000414678.7:c.2576G>C	ENSP00000412835.2:p.Gly859Ala
ENST00000635849.1:c.1739G>C	ENSP00000490948.1:p.Gly580Ala
ENST00000635957.1:c.1370G>C	ENSP00000490385.1:p.Gly457Ala
ENST00000636227.1:n.2881G>C
ENST00000636254.1:n.338G>C
ENST00000636930.2:c.4418G>C MANE Select	ENSP00000490491.2:p.Gly1473Ala
ENST00000636940.1:n.2415G>C
ENST00000637015.1:c.1786G>C
ENST00000637568.1:c.1700G>C
ENST00000637741.1:n.1084G>C
ENST00000637810.1:c.1760G>C	ENSP00000489636.1:p.Gly587Ala
ENST00000637904.1:c.1919G>C	ENSP00000490550.1:p.Gly640Ala
ENST00000647938.1:c.4049G>C	ENSP00000498155.1:p.Gly1350Ala
ENST00000346085.9:c.4049G>C	ENSP00000344546.4:p.Gly1350Ala
ENST00000350026.9:c.4010G>C	ENSP00000055163.7:p.Gly1337Ala
ENST00000414678.6:c.2576G>C	ENSP00000412835.2:p.Gly859Ala
NM_017519.2:c.4010G>C	NP_059989.2:p.Gly1337Ala
NM_020732.3:c.4049G>C	NP_065783.3:p.Gly1350Ala
XM_005267069.3:c.4169G>C	XP_005267126.2:p.Gly1390Ala
XM_011535984.1:c.3248G>C	XP_011534286.1:p.Gly1083Ala
XM_011535985.1:c.3068G>C	XP_011534287.1:p.Gly1023Ala
XM_011535986.1:c.2828G>C	XP_011534288.1:p.Gly943Ala
XM_011535987.1:c.2447G>C	XP_011534289.1:p.Gly816Ala
XM_011535988.1:c.1310G>C	XP_011534290.1:p.Gly437Ala
NM_001346813.1:c.4169G>C	NP_001333742.1:p.Gly1390Ala
NM_001363725.1:c.1919G>C	NP_001350654.1:p.Gly640Ala
XM_011535984.2:c.4379G>C	XP_011534286.2:p.Gly1460Ala
XM_011535988.3:c.1310G>C	XP_011534290.1:p.Gly437Ala
XM_017011103.2:c.4280G>C	XP_016866592.1:p.Gly1427Ala
XM_017011104.1:c.4250G>C	XP_016866593.1:p.Gly1417Ala
XM_017011105.2:c.4220G>C	XP_016866594.1:p.Gly1407Ala
XM_017011106.2:c.4091G>C	XP_016866595.1:p.Gly1364Ala
XM_017011107.2:c.4070G>C	XP_016866596.1:p.Gly1357Ala
XR_002956289.1:n.4427-1859G>C
NM_001363725.2:c.1919G>C	NP_001350654.1:p.Gly640Ala
NM_001371656.1:c.4298G>C	NP_001358585.1:p.Gly1433Ala
NM_001374820.1:c.4298G>C	NP_001361749.1:p.Gly1433Ala
NM_001374828.1:c.4418G>C MANE Select	NP_001361757.1:p.Gly1473Ala
NM_017519.3:c.4259G>C	NP_059989.3:p.Gly1420Ala