Canonical Allele Identifier: CA366242415

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522423C>G (hg19) ; chr6:g.157201289C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201289C>G , CM000668.2:g.157201289C>G	GRCh38
NC_000006.11:g.157522423C>G , CM000668.1:g.157522423C>G	GRCh37
NC_000006.10:g.157564115C>G	NCBI36
NG_032093.1:g.428360C>G
NG_032093.2:g.428360C>G
NG_066624.1:g.430264C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4905C>G	ENSP00000055163.8:p.Asn1635Lys
ENST00000414678.8:c.4974C>G	ENSP00000412835.3:p.Asn1658Lys
ENST00000637015.2:c.5193C>G	ENSP00000489729.2:p.Asn1731Lys
ENST00000346085.10:c.4944C>G	ENSP00000344546.5:p.Asn1648Lys
ENST00000350026.10:c.4656C>G	ENSP00000055163.7:p.Asn1552Lys
ENST00000414678.7:c.3222C>G	ENSP00000412835.2:p.Asn1074Lys
ENST00000635849.1:c.2385C>G	ENSP00000490948.1:p.Asn795Lys
ENST00000635957.1:c.2016C>G	ENSP00000490385.1:p.Asn672Lys
ENST00000636227.1:n.3527C>G
ENST00000636254.1:n.984C>G
ENST00000636930.2:c.5064C>G MANE Select	ENSP00000490491.2:p.Asn1688Lys
ENST00000636940.1:n.3061C>G
ENST00000637015.1:c.2432C>G
ENST00000637568.1:c.2346C>G
ENST00000637741.1:n.1730C>G
ENST00000637810.1:c.2406C>G	ENSP00000489636.1:p.Asn802Lys
ENST00000637904.1:c.2565C>G	ENSP00000490550.1:p.Asn855Lys
ENST00000647938.1:c.4695C>G	ENSP00000498155.1:p.Asn1565Lys
ENST00000346085.9:c.4695C>G	ENSP00000344546.4:p.Asn1565Lys
ENST00000350026.9:c.4656C>G	ENSP00000055163.7:p.Asn1552Lys
ENST00000414678.6:c.3222C>G	ENSP00000412835.2:p.Asn1074Lys
NM_017519.2:c.4656C>G	NP_059989.2:p.Asn1552Lys
NM_020732.3:c.4695C>G	NP_065783.3:p.Asn1565Lys
XM_005267069.3:c.4815C>G	XP_005267126.2:p.Asn1605Lys
XM_011535984.1:c.3894C>G	XP_011534286.1:p.Asn1298Lys
XM_011535985.1:c.3714C>G	XP_011534287.1:p.Asn1238Lys
XM_011535986.1:c.3474C>G	XP_011534288.1:p.Asn1158Lys
XM_011535987.1:c.3093C>G	XP_011534289.1:p.Asn1031Lys
XM_011535988.1:c.1956C>G	XP_011534290.1:p.Asn652Lys
NM_001346813.1:c.4815C>G	NP_001333742.1:p.Asn1605Lys
NM_001363725.1:c.2565C>G	NP_001350654.1:p.Asn855Lys
XM_011535984.2:c.5025C>G	XP_011534286.2:p.Asn1675Lys
XM_011535988.3:c.1956C>G	XP_011534290.1:p.Asn652Lys
XM_017011103.2:c.4926C>G	XP_016866592.1:p.Asn1642Lys
XM_017011104.1:c.4896C>G	XP_016866593.1:p.Asn1632Lys
XM_017011105.2:c.4866C>G	XP_016866594.1:p.Asn1622Lys
XM_017011106.2:c.4737C>G	XP_016866595.1:p.Asn1579Lys
XM_017011107.2:c.4716C>G	XP_016866596.1:p.Asn1572Lys
XR_002956289.1:n.5011C>G
NM_001363725.2:c.2565C>G	NP_001350654.1:p.Asn855Lys
NM_001371656.1:c.4944C>G	NP_001358585.1:p.Asn1648Lys
NM_001374820.1:c.4944C>G	NP_001361749.1:p.Asn1648Lys
NM_001374828.1:c.5064C>G MANE Select	NP_001361757.1:p.Asn1688Lys
NM_017519.3:c.4905C>G	NP_059989.3:p.Asn1635Lys