Canonical Allele Identifier: CA150370233

Gene: ARID1B

Linked Data

• dbSNP Id: rs980714829
• MyVariant Identifiers: chr6:g.157522247A>G (hg19) ; chr6:g.157201113A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201113A>G , CM000668.2:g.157201113A>G	GRCh38
NC_000006.11:g.157522247A>G , CM000668.1:g.157522247A>G	GRCh37
NC_000006.10:g.157563939A>G	NCBI36
NG_032093.1:g.428184A>G
NG_032093.2:g.428184A>G
NG_066624.1:g.430088A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4729A>G	ENSP00000055163.8:p.Asn1577Asp
ENST00000414678.8:c.4798A>G	ENSP00000412835.3:p.Asn1600Asp
ENST00000637015.2:c.5017A>G	ENSP00000489729.2:p.Asn1673Asp
ENST00000346085.10:c.4768A>G	ENSP00000344546.5:p.Asn1590Asp
ENST00000350026.10:c.4480A>G	ENSP00000055163.7:p.Asn1494Asp
ENST00000414678.7:c.3046A>G	ENSP00000412835.2:p.Asn1016Asp
ENST00000635849.1:c.2209A>G	ENSP00000490948.1:p.Asn737Asp
ENST00000635957.1:c.1840A>G	ENSP00000490385.1:p.Asn614Asp
ENST00000636227.1:n.3351A>G
ENST00000636254.1:n.808A>G
ENST00000636930.2:c.4888A>G MANE Select	ENSP00000490491.2:p.Asn1630Asp
ENST00000636940.1:n.2885A>G
ENST00000637015.1:c.2256A>G
ENST00000637568.1:c.2170A>G
ENST00000637741.1:n.1554A>G
ENST00000637810.1:c.2230A>G	ENSP00000489636.1:p.Asn744Asp
ENST00000637904.1:c.2389A>G	ENSP00000490550.1:p.Asn797Asp
ENST00000647938.1:c.4519A>G	ENSP00000498155.1:p.Asn1507Asp
ENST00000346085.9:c.4519A>G	ENSP00000344546.4:p.Asn1507Asp
ENST00000350026.9:c.4480A>G	ENSP00000055163.7:p.Asn1494Asp
ENST00000414678.6:c.3046A>G	ENSP00000412835.2:p.Asn1016Asp
NM_017519.2:c.4480A>G	NP_059989.2:p.Asn1494Asp
NM_020732.3:c.4519A>G	NP_065783.3:p.Asn1507Asp
XM_005267069.3:c.4639A>G	XP_005267126.2:p.Asn1547Asp
XM_011535984.1:c.3718A>G	XP_011534286.1:p.Asn1240Asp
XM_011535985.1:c.3538A>G	XP_011534287.1:p.Asn1180Asp
XM_011535986.1:c.3298A>G	XP_011534288.1:p.Asn1100Asp
XM_011535987.1:c.2917A>G	XP_011534289.1:p.Asn973Asp
XM_011535988.1:c.1780A>G	XP_011534290.1:p.Asn594Asp
NM_001346813.1:c.4639A>G	NP_001333742.1:p.Asn1547Asp
NM_001363725.1:c.2389A>G	NP_001350654.1:p.Asn797Asp
XM_011535984.2:c.4849A>G	XP_011534286.2:p.Asn1617Asp
XM_011535988.3:c.1780A>G	XP_011534290.1:p.Asn594Asp
XM_017011103.2:c.4750A>G	XP_016866592.1:p.Asn1584Asp
XM_017011104.1:c.4720A>G	XP_016866593.1:p.Asn1574Asp
XM_017011105.2:c.4690A>G	XP_016866594.1:p.Asn1564Asp
XM_017011106.2:c.4561A>G	XP_016866595.1:p.Asn1521Asp
XM_017011107.2:c.4540A>G	XP_016866596.1:p.Asn1514Asp
XR_002956289.1:n.4835A>G
NM_001363725.2:c.2389A>G	NP_001350654.1:p.Asn797Asp
NM_001371656.1:c.4768A>G	NP_001358585.1:p.Asn1590Asp
NM_001374820.1:c.4768A>G	NP_001361749.1:p.Asn1590Asp
NM_001374828.1:c.4888A>G MANE Select	NP_001361757.1:p.Asn1630Asp
NM_017519.3:c.4729A>G	NP_059989.3:p.Asn1577Asp