Canonical Allele Identifier: CA366242958

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2055772
• ClinVar RCV Id: RCV002910128
• dbSNP Id: rs1206706709
• gnomAD v4: 6-157201405-G-A
• MyVariant Identifiers: chr6:g.157522539G>A (hg19) ; chr6:g.157201405G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201405G>A , CM000668.2:g.157201405G>A	GRCh38
NC_000006.11:g.157522539G>A , CM000668.1:g.157522539G>A	GRCh37
NC_000006.10:g.157564231G>A	NCBI36
NG_032093.1:g.428476G>A
NG_032093.2:g.428476G>A
NG_066624.1:g.430380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5021G>A	ENSP00000055163.8:p.Arg1674Lys
ENST00000414678.8:c.5090G>A	ENSP00000412835.3:p.Arg1697Lys
ENST00000637015.2:c.5309G>A	ENSP00000489729.2:p.Arg1770Lys
ENST00000346085.10:c.5060G>A	ENSP00000344546.5:p.Arg1687Lys
ENST00000350026.10:c.4772G>A	ENSP00000055163.7:p.Arg1591Lys
ENST00000414678.7:c.3338G>A	ENSP00000412835.2:p.Arg1113Lys
ENST00000635849.1:c.2501G>A	ENSP00000490948.1:p.Arg834Lys
ENST00000635957.1:c.2132G>A	ENSP00000490385.1:p.Arg711Lys
ENST00000636227.1:n.3643G>A
ENST00000636254.1:n.1100G>A
ENST00000636930.2:c.5180G>A MANE Select	ENSP00000490491.2:p.Arg1727Lys
ENST00000636940.1:n.3177G>A
ENST00000637015.1:c.2548G>A
ENST00000637568.1:c.2462G>A
ENST00000637741.1:n.1846G>A
ENST00000637810.1:c.2522G>A	ENSP00000489636.1:p.Arg841Lys
ENST00000637904.1:c.2681G>A	ENSP00000490550.1:p.Arg894Lys
ENST00000647938.1:c.4811G>A	ENSP00000498155.1:p.Arg1604Lys
ENST00000346085.9:c.4811G>A	ENSP00000344546.4:p.Arg1604Lys
ENST00000350026.9:c.4772G>A	ENSP00000055163.7:p.Arg1591Lys
ENST00000414678.6:c.3338G>A	ENSP00000412835.2:p.Arg1113Lys
NM_017519.2:c.4772G>A	NP_059989.2:p.Arg1591Lys
NM_020732.3:c.4811G>A	NP_065783.3:p.Arg1604Lys
XM_005267069.3:c.4931G>A	XP_005267126.2:p.Arg1644Lys
XM_011535984.1:c.4010G>A	XP_011534286.1:p.Arg1337Lys
XM_011535985.1:c.3830G>A	XP_011534287.1:p.Arg1277Lys
XM_011535986.1:c.3590G>A	XP_011534288.1:p.Arg1197Lys
XM_011535987.1:c.3209G>A	XP_011534289.1:p.Arg1070Lys
XM_011535988.1:c.2072G>A	XP_011534290.1:p.Arg691Lys
NM_001346813.1:c.4931G>A	NP_001333742.1:p.Arg1644Lys
NM_001363725.1:c.2681G>A	NP_001350654.1:p.Arg894Lys
XM_011535984.2:c.5141G>A	XP_011534286.2:p.Arg1714Lys
XM_011535988.3:c.2072G>A	XP_011534290.1:p.Arg691Lys
XM_017011103.2:c.5042G>A	XP_016866592.1:p.Arg1681Lys
XM_017011104.1:c.5012G>A	XP_016866593.1:p.Arg1671Lys
XM_017011105.2:c.4982G>A	XP_016866594.1:p.Arg1661Lys
XM_017011106.2:c.4853G>A	XP_016866595.1:p.Arg1618Lys
XM_017011107.2:c.4832G>A	XP_016866596.1:p.Arg1611Lys
XR_002956289.1:n.5127G>A
NM_001363725.2:c.2681G>A	NP_001350654.1:p.Arg894Lys
NM_001371656.1:c.5060G>A	NP_001358585.1:p.Arg1687Lys
NM_001374820.1:c.5060G>A	NP_001361749.1:p.Arg1687Lys
NM_001374828.1:c.5180G>A MANE Select	NP_001361757.1:p.Arg1727Lys
NM_017519.3:c.5021G>A	NP_059989.3:p.Arg1674Lys