Canonical Allele Identifier: CA366241304

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522089C>G (hg19) ; chr6:g.157200955C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200955C>G , CM000668.2:g.157200955C>G	GRCh38
NC_000006.11:g.157522089C>G , CM000668.1:g.157522089C>G	GRCh37
NC_000006.10:g.157563781C>G	NCBI36
NG_032093.1:g.428026C>G
NG_032093.2:g.428026C>G
NG_066624.1:g.429930C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4571C>G	ENSP00000055163.8:p.Ser1524Trp
ENST00000414678.8:c.4640C>G	ENSP00000412835.3:p.Ser1547Trp
ENST00000637015.2:c.4859C>G	ENSP00000489729.2:p.Ser1620Trp
ENST00000346085.10:c.4610C>G	ENSP00000344546.5:p.Ser1537Trp
ENST00000350026.10:c.4322C>G	ENSP00000055163.7:p.Ser1441Trp
ENST00000414678.7:c.2888C>G	ENSP00000412835.2:p.Ser963Trp
ENST00000635849.1:c.2051C>G	ENSP00000490948.1:p.Ser684Trp
ENST00000635957.1:c.1682C>G	ENSP00000490385.1:p.Ser561Trp
ENST00000636227.1:n.3193C>G
ENST00000636254.1:n.650C>G
ENST00000636930.2:c.4730C>G MANE Select	ENSP00000490491.2:p.Ser1577Trp
ENST00000636940.1:n.2727C>G
ENST00000637015.1:c.2098C>G
ENST00000637568.1:c.2012C>G
ENST00000637741.1:n.1396C>G
ENST00000637810.1:c.2072C>G	ENSP00000489636.1:p.Ser691Trp
ENST00000637904.1:c.2231C>G	ENSP00000490550.1:p.Ser744Trp
ENST00000647938.1:c.4361C>G	ENSP00000498155.1:p.Ser1454Trp
ENST00000346085.9:c.4361C>G	ENSP00000344546.4:p.Ser1454Trp
ENST00000350026.9:c.4322C>G	ENSP00000055163.7:p.Ser1441Trp
ENST00000414678.6:c.2888C>G	ENSP00000412835.2:p.Ser963Trp
NM_017519.2:c.4322C>G	NP_059989.2:p.Ser1441Trp
NM_020732.3:c.4361C>G	NP_065783.3:p.Ser1454Trp
XM_005267069.3:c.4481C>G	XP_005267126.2:p.Ser1494Trp
XM_011535984.1:c.3560C>G	XP_011534286.1:p.Ser1187Trp
XM_011535985.1:c.3380C>G	XP_011534287.1:p.Ser1127Trp
XM_011535986.1:c.3140C>G	XP_011534288.1:p.Ser1047Trp
XM_011535987.1:c.2759C>G	XP_011534289.1:p.Ser920Trp
XM_011535988.1:c.1622C>G	XP_011534290.1:p.Ser541Trp
NM_001346813.1:c.4481C>G	NP_001333742.1:p.Ser1494Trp
NM_001363725.1:c.2231C>G	NP_001350654.1:p.Ser744Trp
XM_011535984.2:c.4691C>G	XP_011534286.2:p.Ser1564Trp
XM_011535988.3:c.1622C>G	XP_011534290.1:p.Ser541Trp
XM_017011103.2:c.4592C>G	XP_016866592.1:p.Ser1531Trp
XM_017011104.1:c.4562C>G	XP_016866593.1:p.Ser1521Trp
XM_017011105.2:c.4532C>G	XP_016866594.1:p.Ser1511Trp
XM_017011106.2:c.4403C>G	XP_016866595.1:p.Ser1468Trp
XM_017011107.2:c.4382C>G	XP_016866596.1:p.Ser1461Trp
XR_002956289.1:n.4677C>G
NM_001363725.2:c.2231C>G	NP_001350654.1:p.Ser744Trp
NM_001371656.1:c.4610C>G	NP_001358585.1:p.Ser1537Trp
NM_001374820.1:c.4610C>G	NP_001361749.1:p.Ser1537Trp
NM_001374828.1:c.4730C>G MANE Select	NP_001361757.1:p.Ser1577Trp
NM_017519.3:c.4571C>G	NP_059989.3:p.Ser1524Trp