Canonical Allele Identifier: CA366241929

Gene: ARID1B

Linked Data

• dbSNP Id: rs34870395
• gnomAD v4: 6-157201089-A-G
• MyVariant Identifiers: chr6:g.157522223A>G (hg19) ; chr6:g.157201089A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201089A>G , CM000668.2:g.157201089A>G	GRCh38
NC_000006.11:g.157522223A>G , CM000668.1:g.157522223A>G	GRCh37
NC_000006.10:g.157563915A>G	NCBI36
NG_032093.1:g.428160A>G
NG_032093.2:g.428160A>G
NG_066624.1:g.430064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4705A>G	ENSP00000055163.8:p.Met1569Val
ENST00000414678.8:c.4774A>G	ENSP00000412835.3:p.Met1592Val
ENST00000637015.2:c.4993A>G	ENSP00000489729.2:p.Met1665Val
ENST00000346085.10:c.4744A>G	ENSP00000344546.5:p.Met1582Val
ENST00000350026.10:c.4456A>G	ENSP00000055163.7:p.Met1486Val
ENST00000414678.7:c.3022A>G	ENSP00000412835.2:p.Met1008Val
ENST00000635849.1:c.2185A>G	ENSP00000490948.1:p.Met729Val
ENST00000635957.1:c.1816A>G	ENSP00000490385.1:p.Met606Val
ENST00000636227.1:n.3327A>G
ENST00000636254.1:n.784A>G
ENST00000636930.2:c.4864A>G MANE Select	ENSP00000490491.2:p.Met1622Val
ENST00000636940.1:n.2861A>G
ENST00000637015.1:c.2232A>G
ENST00000637568.1:c.2146A>G
ENST00000637741.1:n.1530A>G
ENST00000637810.1:c.2206A>G	ENSP00000489636.1:p.Met736Val
ENST00000637904.1:c.2365A>G	ENSP00000490550.1:p.Met789Val
ENST00000647938.1:c.4495A>G	ENSP00000498155.1:p.Met1499Val
ENST00000346085.9:c.4495A>G	ENSP00000344546.4:p.Met1499Val
ENST00000350026.9:c.4456A>G	ENSP00000055163.7:p.Met1486Val
ENST00000414678.6:c.3022A>G	ENSP00000412835.2:p.Met1008Val
NM_017519.2:c.4456A>G	NP_059989.2:p.Met1486Val
NM_020732.3:c.4495A>G	NP_065783.3:p.Met1499Val
XM_005267069.3:c.4615A>G	XP_005267126.2:p.Met1539Val
XM_011535984.1:c.3694A>G	XP_011534286.1:p.Met1232Val
XM_011535985.1:c.3514A>G	XP_011534287.1:p.Met1172Val
XM_011535986.1:c.3274A>G	XP_011534288.1:p.Met1092Val
XM_011535987.1:c.2893A>G	XP_011534289.1:p.Met965Val
XM_011535988.1:c.1756A>G	XP_011534290.1:p.Met586Val
NM_001346813.1:c.4615A>G	NP_001333742.1:p.Met1539Val
NM_001363725.1:c.2365A>G	NP_001350654.1:p.Met789Val
XM_011535984.2:c.4825A>G	XP_011534286.2:p.Met1609Val
XM_011535988.3:c.1756A>G	XP_011534290.1:p.Met586Val
XM_017011103.2:c.4726A>G	XP_016866592.1:p.Met1576Val
XM_017011104.1:c.4696A>G	XP_016866593.1:p.Met1566Val
XM_017011105.2:c.4666A>G	XP_016866594.1:p.Met1556Val
XM_017011106.2:c.4537A>G	XP_016866595.1:p.Met1513Val
XM_017011107.2:c.4516A>G	XP_016866596.1:p.Met1506Val
XR_002956289.1:n.4811A>G
NM_001363725.2:c.2365A>G	NP_001350654.1:p.Met789Val
NM_001371656.1:c.4744A>G	NP_001358585.1:p.Met1582Val
NM_001374820.1:c.4744A>G	NP_001361749.1:p.Met1582Val
NM_001374828.1:c.4864A>G MANE Select	NP_001361757.1:p.Met1622Val
NM_017519.3:c.4705A>G	NP_059989.3:p.Met1569Val