Canonical Allele Identifier: CA366242264

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375292
• MyVariant Identifiers: chr6:g.157522351G>C (hg19) ; chr6:g.157201217G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201217G>C , CM000668.2:g.157201217G>C	GRCh38
NC_000006.11:g.157522351G>C , CM000668.1:g.157522351G>C	GRCh37
NC_000006.10:g.157564043G>C	NCBI36
NG_032093.1:g.428288G>C
NG_032093.2:g.428288G>C
NG_066624.1:g.430192G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4833G>C	ENSP00000055163.8:p.Gln1611His
ENST00000414678.8:c.4902G>C	ENSP00000412835.3:p.Gln1634His
ENST00000637015.2:c.5121G>C	ENSP00000489729.2:p.Gln1707His
ENST00000346085.10:c.4872G>C	ENSP00000344546.5:p.Gln1624His
ENST00000350026.10:c.4584G>C	ENSP00000055163.7:p.Gln1528His
ENST00000414678.7:c.3150G>C	ENSP00000412835.2:p.Gln1050His
ENST00000635849.1:c.2313G>C	ENSP00000490948.1:p.Gln771His
ENST00000635957.1:c.1944G>C	ENSP00000490385.1:p.Gln648His
ENST00000636227.1:n.3455G>C
ENST00000636254.1:n.912G>C
ENST00000636930.2:c.4992G>C MANE Select	ENSP00000490491.2:p.Gln1664His
ENST00000636940.1:n.2989G>C
ENST00000637015.1:c.2360G>C
ENST00000637568.1:c.2274G>C
ENST00000637741.1:n.1658G>C
ENST00000637810.1:c.2334G>C	ENSP00000489636.1:p.Gln778His
ENST00000637904.1:c.2493G>C	ENSP00000490550.1:p.Gln831His
ENST00000647938.1:c.4623G>C	ENSP00000498155.1:p.Gln1541His
ENST00000346085.9:c.4623G>C	ENSP00000344546.4:p.Gln1541His
ENST00000350026.9:c.4584G>C	ENSP00000055163.7:p.Gln1528His
ENST00000414678.6:c.3150G>C	ENSP00000412835.2:p.Gln1050His
NM_017519.2:c.4584G>C	NP_059989.2:p.Gln1528His
NM_020732.3:c.4623G>C	NP_065783.3:p.Gln1541His
XM_005267069.3:c.4743G>C	XP_005267126.2:p.Gln1581His
XM_011535984.1:c.3822G>C	XP_011534286.1:p.Gln1274His
XM_011535985.1:c.3642G>C	XP_011534287.1:p.Gln1214His
XM_011535986.1:c.3402G>C	XP_011534288.1:p.Gln1134His
XM_011535987.1:c.3021G>C	XP_011534289.1:p.Gln1007His
XM_011535988.1:c.1884G>C	XP_011534290.1:p.Gln628His
NM_001346813.1:c.4743G>C	NP_001333742.1:p.Gln1581His
NM_001363725.1:c.2493G>C	NP_001350654.1:p.Gln831His
XM_011535984.2:c.4953G>C	XP_011534286.2:p.Gln1651His
XM_011535988.3:c.1884G>C	XP_011534290.1:p.Gln628His
XM_017011103.2:c.4854G>C	XP_016866592.1:p.Gln1618His
XM_017011104.1:c.4824G>C	XP_016866593.1:p.Gln1608His
XM_017011105.2:c.4794G>C	XP_016866594.1:p.Gln1598His
XM_017011106.2:c.4665G>C	XP_016866595.1:p.Gln1555His
XM_017011107.2:c.4644G>C	XP_016866596.1:p.Gln1548His
XR_002956289.1:n.4939G>C
NM_001363725.2:c.2493G>C	NP_001350654.1:p.Gln831His
NM_001371656.1:c.4872G>C	NP_001358585.1:p.Gln1624His
NM_001374820.1:c.4872G>C	NP_001361749.1:p.Gln1624His
NM_001374828.1:c.4992G>C MANE Select	NP_001361757.1:p.Gln1664His
NM_017519.3:c.4833G>C	NP_059989.3:p.Gln1611His