Canonical Allele Identifier: CA366387237

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157405904G>T (hg19) ; chr6:g.157084770G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084770G>T , CM000668.2:g.157084770G>T	GRCh38
NC_000006.11:g.157405904G>T , CM000668.1:g.157405904G>T	GRCh37
NC_000006.10:g.157447596G>T	NCBI36
NG_032093.1:g.311841G>T
NG_032093.2:g.311841G>T
NG_066624.1:g.313745G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2356G>T	ENSP00000055163.8:p.Ala786Ser
ENST00000414678.8:c.2356G>T	ENSP00000412835.3:p.Ala786Ser
ENST00000637015.2:c.2356G>T	ENSP00000489729.2:p.Ala786Ser
ENST00000319584.11:c.370G>T	ENSP00000313006.7:p.Ala124Ser
ENST00000346085.10:c.2395G>T	ENSP00000344546.5:p.Ala799Ser
ENST00000350026.10:c.2107G>T	ENSP00000055163.7:p.Ala703Ser
ENST00000414678.7:c.604G>T	ENSP00000412835.2:p.Ala202Ser
ENST00000452544.2:n.257G>T
ENST00000493658.2:n.5G>T
ENST00000635849.1:c.-144G>T	ENSP00000490948.1:n.-144G>T
ENST00000636930.2:c.2356G>T MANE Select	ENSP00000490491.2:p.Ala786Ser
ENST00000637003.1:c.-144G>T	ENSP00000489666.1:n.-144G>T
ENST00000637904.1:c.-144G>T	ENSP00000490550.1:n.-144G>T
ENST00000647938.1:c.2146G>T	ENSP00000498155.1:p.Ala716Ser
ENST00000674190.1:n.1105G>T
ENST00000319584.10:c.373G>T	ENSP00000313006.6:p.Ala125Ser
ENST00000346085.9:c.2146G>T	ENSP00000344546.4:p.Ala716Ser
ENST00000350026.9:c.2107G>T	ENSP00000055163.7:p.Ala703Ser
ENST00000414678.6:c.604G>T	ENSP00000412835.2:p.Ala202Ser
ENST00000452544.1:n.215G>T
ENST00000493658.1:n.5G>T
NM_017519.2:c.2107G>T	NP_059989.2:p.Ala703Ser
NM_020732.3:c.2146G>T	NP_065783.3:p.Ala716Ser
XM_005267069.3:c.2107G>T	XP_005267126.2:p.Ala703Ser
XM_011535984.1:c.1057G>T	XP_011534286.1:p.Ala353Ser
XM_011535985.1:c.1057G>T	XP_011534287.1:p.Ala353Ser
XM_011535986.1:c.637G>T	XP_011534288.1:p.Ala213Ser
XM_011535987.1:c.256G>T	XP_011534289.1:p.Ala86Ser
NM_001346813.1:c.2107G>T	NP_001333742.1:p.Ala703Ser
NM_001363725.1:c.-144G>T	NP_001350654.1:n.-144G>T
XM_011535984.2:c.2188G>T	XP_011534286.2:p.Ala730Ser
XM_017011103.2:c.2188G>T	XP_016866592.1:p.Ala730Ser
XM_017011104.1:c.2188G>T	XP_016866593.1:p.Ala730Ser
XM_017011105.2:c.2188G>T	XP_016866594.1:p.Ala730Ser
XM_017011106.2:c.2188G>T	XP_016866595.1:p.Ala730Ser
XM_017011107.2:c.2188G>T	XP_016866596.1:p.Ala730Ser
XR_002956289.1:n.2271G>T
NM_001363725.2:c.-144G>T	NP_001350654.1:n.-144G>T
NM_001371656.1:c.2395G>T	NP_001358585.1:p.Ala799Ser
NM_001374820.1:c.2395G>T	NP_001361749.1:p.Ala799Ser
NM_001374828.1:c.2356G>T MANE Select	NP_001361757.1:p.Ala786Ser
NM_017519.3:c.2356G>T	NP_059989.3:p.Ala786Ser