Canonical Allele Identifier: CA366242029

Gene: ARID1B

Linked Data

• dbSNP Id: rs1562346118
• MyVariant Identifiers: chr6:g.157522248A>G (hg19) ; chr6:g.157201114A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201114A>G , CM000668.2:g.157201114A>G	GRCh38
NC_000006.11:g.157522248A>G , CM000668.1:g.157522248A>G	GRCh37
NC_000006.10:g.157563940A>G	NCBI36
NG_032093.1:g.428185A>G
NG_032093.2:g.428185A>G
NG_066624.1:g.430089A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4730A>G	ENSP00000055163.8:p.Asn1577Ser
ENST00000414678.8:c.4799A>G	ENSP00000412835.3:p.Asn1600Ser
ENST00000637015.2:c.5018A>G	ENSP00000489729.2:p.Asn1673Ser
ENST00000346085.10:c.4769A>G	ENSP00000344546.5:p.Asn1590Ser
ENST00000350026.10:c.4481A>G	ENSP00000055163.7:p.Asn1494Ser
ENST00000414678.7:c.3047A>G	ENSP00000412835.2:p.Asn1016Ser
ENST00000635849.1:c.2210A>G	ENSP00000490948.1:p.Asn737Ser
ENST00000635957.1:c.1841A>G	ENSP00000490385.1:p.Asn614Ser
ENST00000636227.1:n.3352A>G
ENST00000636254.1:n.809A>G
ENST00000636930.2:c.4889A>G MANE Select	ENSP00000490491.2:p.Asn1630Ser
ENST00000636940.1:n.2886A>G
ENST00000637015.1:c.2257A>G
ENST00000637568.1:c.2171A>G
ENST00000637741.1:n.1555A>G
ENST00000637810.1:c.2231A>G	ENSP00000489636.1:p.Asn744Ser
ENST00000637904.1:c.2390A>G	ENSP00000490550.1:p.Asn797Ser
ENST00000647938.1:c.4520A>G	ENSP00000498155.1:p.Asn1507Ser
ENST00000346085.9:c.4520A>G	ENSP00000344546.4:p.Asn1507Ser
ENST00000350026.9:c.4481A>G	ENSP00000055163.7:p.Asn1494Ser
ENST00000414678.6:c.3047A>G	ENSP00000412835.2:p.Asn1016Ser
NM_017519.2:c.4481A>G	NP_059989.2:p.Asn1494Ser
NM_020732.3:c.4520A>G	NP_065783.3:p.Asn1507Ser
XM_005267069.3:c.4640A>G	XP_005267126.2:p.Asn1547Ser
XM_011535984.1:c.3719A>G	XP_011534286.1:p.Asn1240Ser
XM_011535985.1:c.3539A>G	XP_011534287.1:p.Asn1180Ser
XM_011535986.1:c.3299A>G	XP_011534288.1:p.Asn1100Ser
XM_011535987.1:c.2918A>G	XP_011534289.1:p.Asn973Ser
XM_011535988.1:c.1781A>G	XP_011534290.1:p.Asn594Ser
NM_001346813.1:c.4640A>G	NP_001333742.1:p.Asn1547Ser
NM_001363725.1:c.2390A>G	NP_001350654.1:p.Asn797Ser
XM_011535984.2:c.4850A>G	XP_011534286.2:p.Asn1617Ser
XM_011535988.3:c.1781A>G	XP_011534290.1:p.Asn594Ser
XM_017011103.2:c.4751A>G	XP_016866592.1:p.Asn1584Ser
XM_017011104.1:c.4721A>G	XP_016866593.1:p.Asn1574Ser
XM_017011105.2:c.4691A>G	XP_016866594.1:p.Asn1564Ser
XM_017011106.2:c.4562A>G	XP_016866595.1:p.Asn1521Ser
XM_017011107.2:c.4541A>G	XP_016866596.1:p.Asn1514Ser
XR_002956289.1:n.4836A>G
NM_001363725.2:c.2390A>G	NP_001350654.1:p.Asn797Ser
NM_001371656.1:c.4769A>G	NP_001358585.1:p.Asn1590Ser
NM_001374820.1:c.4769A>G	NP_001361749.1:p.Asn1590Ser
NM_001374828.1:c.4889A>G MANE Select	NP_001361757.1:p.Asn1630Ser
NM_017519.3:c.4730A>G	NP_059989.3:p.Asn1577Ser