Canonical Allele Identifier: CA366242862

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376464
• gnomAD v4: 6-157201387-A-C
• MyVariant Identifiers: chr6:g.157522521A>C (hg19) ; chr6:g.157201387A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201387A>C , CM000668.2:g.157201387A>C	GRCh38
NC_000006.11:g.157522521A>C , CM000668.1:g.157522521A>C	GRCh37
NC_000006.10:g.157564213A>C	NCBI36
NG_032093.1:g.428458A>C
NG_032093.2:g.428458A>C
NG_066624.1:g.430362A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5003A>C	ENSP00000055163.8:p.Gln1668Pro
ENST00000414678.8:c.5072A>C	ENSP00000412835.3:p.Gln1691Pro
ENST00000637015.2:c.5291A>C	ENSP00000489729.2:p.Gln1764Pro
ENST00000346085.10:c.5042A>C	ENSP00000344546.5:p.Gln1681Pro
ENST00000350026.10:c.4754A>C	ENSP00000055163.7:p.Gln1585Pro
ENST00000414678.7:c.3320A>C	ENSP00000412835.2:p.Gln1107Pro
ENST00000635849.1:c.2483A>C	ENSP00000490948.1:p.Gln828Pro
ENST00000635957.1:c.2114A>C	ENSP00000490385.1:p.Gln705Pro
ENST00000636227.1:n.3625A>C
ENST00000636254.1:n.1082A>C
ENST00000636930.2:c.5162A>C MANE Select	ENSP00000490491.2:p.Gln1721Pro
ENST00000636940.1:n.3159A>C
ENST00000637015.1:c.2530A>C
ENST00000637568.1:c.2444A>C
ENST00000637741.1:n.1828A>C
ENST00000637810.1:c.2504A>C	ENSP00000489636.1:p.Gln835Pro
ENST00000637904.1:c.2663A>C	ENSP00000490550.1:p.Gln888Pro
ENST00000647938.1:c.4793A>C	ENSP00000498155.1:p.Gln1598Pro
ENST00000346085.9:c.4793A>C	ENSP00000344546.4:p.Gln1598Pro
ENST00000350026.9:c.4754A>C	ENSP00000055163.7:p.Gln1585Pro
ENST00000414678.6:c.3320A>C	ENSP00000412835.2:p.Gln1107Pro
NM_017519.2:c.4754A>C	NP_059989.2:p.Gln1585Pro
NM_020732.3:c.4793A>C	NP_065783.3:p.Gln1598Pro
XM_005267069.3:c.4913A>C	XP_005267126.2:p.Gln1638Pro
XM_011535984.1:c.3992A>C	XP_011534286.1:p.Gln1331Pro
XM_011535985.1:c.3812A>C	XP_011534287.1:p.Gln1271Pro
XM_011535986.1:c.3572A>C	XP_011534288.1:p.Gln1191Pro
XM_011535987.1:c.3191A>C	XP_011534289.1:p.Gln1064Pro
XM_011535988.1:c.2054A>C	XP_011534290.1:p.Gln685Pro
NM_001346813.1:c.4913A>C	NP_001333742.1:p.Gln1638Pro
NM_001363725.1:c.2663A>C	NP_001350654.1:p.Gln888Pro
XM_011535984.2:c.5123A>C	XP_011534286.2:p.Gln1708Pro
XM_011535988.3:c.2054A>C	XP_011534290.1:p.Gln685Pro
XM_017011103.2:c.5024A>C	XP_016866592.1:p.Gln1675Pro
XM_017011104.1:c.4994A>C	XP_016866593.1:p.Gln1665Pro
XM_017011105.2:c.4964A>C	XP_016866594.1:p.Gln1655Pro
XM_017011106.2:c.4835A>C	XP_016866595.1:p.Gln1612Pro
XM_017011107.2:c.4814A>C	XP_016866596.1:p.Gln1605Pro
XR_002956289.1:n.5109A>C
NM_001363725.2:c.2663A>C	NP_001350654.1:p.Gln888Pro
NM_001371656.1:c.5042A>C	NP_001358585.1:p.Gln1681Pro
NM_001374820.1:c.5042A>C	NP_001361749.1:p.Gln1681Pro
NM_001374828.1:c.5162A>C MANE Select	NP_001361757.1:p.Gln1721Pro
NM_017519.3:c.5003A>C	NP_059989.3:p.Gln1668Pro