Canonical Allele Identifier: CA366387436

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128463319
• MyVariant Identifiers: chr6:g.157406009T>A (hg19) ; chr6:g.157084875T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084875T>A , CM000668.2:g.157084875T>A	GRCh38
NC_000006.11:g.157406009T>A , CM000668.1:g.157406009T>A	GRCh37
NC_000006.10:g.157447701T>A	NCBI36
NG_032093.1:g.311946T>A
NG_032093.2:g.311946T>A
NG_066624.1:g.313850T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2461T>A	ENSP00000055163.8:p.Ser821Thr
ENST00000414678.8:c.2461T>A	ENSP00000412835.3:p.Ser821Thr
ENST00000637015.2:c.2461T>A	ENSP00000489729.2:p.Ser821Thr
ENST00000319584.11:c.475T>A	ENSP00000313006.7:p.Ser159Thr
ENST00000346085.10:c.2500T>A	ENSP00000344546.5:p.Ser834Thr
ENST00000350026.10:c.2212T>A	ENSP00000055163.7:p.Ser738Thr
ENST00000414678.7:c.709T>A	ENSP00000412835.2:p.Ser237Thr
ENST00000452544.2:n.362T>A
ENST00000493658.2:n.110T>A
ENST00000635849.1:c.-39T>A	ENSP00000490948.1:n.-39T>A
ENST00000636930.2:c.2461T>A MANE Select	ENSP00000490491.2:p.Ser821Thr
ENST00000637003.1:c.-39T>A	ENSP00000489666.1:n.-39T>A
ENST00000637810.1:c.-39T>A	ENSP00000489636.1:n.-39T>A
ENST00000637904.1:c.-39T>A	ENSP00000490550.1:n.-39T>A
ENST00000647938.1:c.2251T>A	ENSP00000498155.1:p.Ser751Thr
ENST00000674190.1:n.1210T>A
ENST00000319584.10:c.478T>A	ENSP00000313006.6:p.Ser160Thr
ENST00000346085.9:c.2251T>A	ENSP00000344546.4:p.Ser751Thr
ENST00000350026.9:c.2212T>A	ENSP00000055163.7:p.Ser738Thr
ENST00000414678.6:c.709T>A	ENSP00000412835.2:p.Ser237Thr
ENST00000452544.1:n.320T>A
ENST00000493658.1:n.110T>A
NM_017519.2:c.2212T>A	NP_059989.2:p.Ser738Thr
NM_020732.3:c.2251T>A	NP_065783.3:p.Ser751Thr
XM_005267069.3:c.2212T>A	XP_005267126.2:p.Ser738Thr
XM_011535984.1:c.1162T>A	XP_011534286.1:p.Ser388Thr
XM_011535985.1:c.1162T>A	XP_011534287.1:p.Ser388Thr
XM_011535986.1:c.742T>A	XP_011534288.1:p.Ser248Thr
XM_011535987.1:c.361T>A	XP_011534289.1:p.Ser121Thr
NM_001346813.1:c.2212T>A	NP_001333742.1:p.Ser738Thr
NM_001363725.1:c.-39T>A	NP_001350654.1:n.-39T>A
XM_011535984.2:c.2293T>A	XP_011534286.2:p.Ser765Thr
XM_017011103.2:c.2293T>A	XP_016866592.1:p.Ser765Thr
XM_017011104.1:c.2293T>A	XP_016866593.1:p.Ser765Thr
XM_017011105.2:c.2293T>A	XP_016866594.1:p.Ser765Thr
XM_017011106.2:c.2293T>A	XP_016866595.1:p.Ser765Thr
XM_017011107.2:c.2293T>A	XP_016866596.1:p.Ser765Thr
XR_002956289.1:n.2376T>A
NM_001363725.2:c.-39T>A	NP_001350654.1:n.-39T>A
NM_001371656.1:c.2500T>A	NP_001358585.1:p.Ser834Thr
NM_001374820.1:c.2500T>A	NP_001361749.1:p.Ser834Thr
NM_001374828.1:c.2461T>A MANE Select	NP_001361757.1:p.Ser821Thr
NM_017519.3:c.2461T>A	NP_059989.3:p.Ser821Thr