Canonical Allele Identifier: CA366389277

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470070A>G (hg19) ; chr6:g.157148936A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148936A>G , CM000668.2:g.157148936A>G	GRCh38
NC_000006.11:g.157470070A>G , CM000668.1:g.157470070A>G	GRCh37
NC_000006.10:g.157511762A>G	NCBI36
NG_032093.1:g.376007A>G
NG_032093.2:g.376007A>G
NG_066624.1:g.377911A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3074A>G	ENSP00000055163.8:p.Asn1025Ser
ENST00000414678.8:c.2984A>G	ENSP00000412835.3:p.Asn995Ser
ENST00000637015.2:c.3074A>G	ENSP00000489729.2:p.Asn1025Ser
ENST00000319584.11:c.1088A>G	ENSP00000313006.7:p.Asn363Ser
ENST00000346085.10:c.3113A>G	ENSP00000344546.5:p.Asn1038Ser
ENST00000350026.10:c.2825A>G	ENSP00000055163.7:p.Asn942Ser
ENST00000414678.7:c.1232A>G	ENSP00000412835.2:p.Asn411Ser
ENST00000452544.2:n.975A>G
ENST00000635849.1:c.395A>G	ENSP00000490948.1:p.Asn132Ser
ENST00000635957.1:c.29A>G	ENSP00000490385.1:p.Asn10Ser
ENST00000636426.1:n.208A>G
ENST00000636930.2:c.3074A>G MANE Select	ENSP00000490491.2:p.Asn1025Ser
ENST00000637015.1:c.313A>G
ENST00000637568.1:c.117A>G
ENST00000637810.1:c.575A>G	ENSP00000489636.1:p.Asn192Ser
ENST00000637904.1:c.575A>G	ENSP00000490550.1:p.Asn192Ser
ENST00000647938.1:c.2864A>G	ENSP00000498155.1:p.Asn955Ser
ENST00000674190.1:n.1823A>G
ENST00000319584.10:c.1091A>G	ENSP00000313006.6:p.Asn364Ser
ENST00000346085.9:c.2864A>G	ENSP00000344546.4:p.Asn955Ser
ENST00000350026.9:c.2825A>G	ENSP00000055163.7:p.Asn942Ser
ENST00000400790.3:c.26A>G	ENSP00000383596.3:p.Asn9Ser
ENST00000414678.6:c.1232A>G	ENSP00000412835.2:p.Asn411Ser
ENST00000452544.1:n.921A>G
ENST00000478761.3:c.147A>G
NM_017519.2:c.2825A>G	NP_059989.2:p.Asn942Ser
NM_020732.3:c.2864A>G	NP_065783.3:p.Asn955Ser
XM_005267069.3:c.2825A>G	XP_005267126.2:p.Asn942Ser
XM_011535984.1:c.1775A>G	XP_011534286.1:p.Asn592Ser
XM_011535985.1:c.1595A>G	XP_011534287.1:p.Asn532Ser
XM_011535986.1:c.1355A>G	XP_011534288.1:p.Asn452Ser
XM_011535987.1:c.974A>G	XP_011534289.1:p.Asn325Ser
XM_011535988.1:c.-20+15729A>G	XP_011534290.1:n.-20+15729A>G
NM_001346813.1:c.2825A>G	NP_001333742.1:p.Asn942Ser
NM_001363725.1:c.575A>G	NP_001350654.1:p.Asn192Ser
XM_011535984.2:c.2906A>G	XP_011534286.2:p.Asn969Ser
XM_011535988.3:c.-20+15729A>G	XP_011534290.1:n.-20+15729A>G
XM_017011103.2:c.2906A>G	XP_016866592.1:p.Asn969Ser
XM_017011104.1:c.2906A>G	XP_016866593.1:p.Asn969Ser
XM_017011105.2:c.2906A>G	XP_016866594.1:p.Asn969Ser
XM_017011106.2:c.2906A>G	XP_016866595.1:p.Asn969Ser
XM_017011107.2:c.2726A>G	XP_016866596.1:p.Asn909Ser
XR_002956289.1:n.2989A>G
NM_001363725.2:c.575A>G	NP_001350654.1:p.Asn192Ser
NM_001371656.1:c.3113A>G	NP_001358585.1:p.Asn1038Ser
NM_001374820.1:c.3113A>G	NP_001361749.1:p.Asn1038Ser
NM_001374828.1:c.3074A>G MANE Select	NP_001361757.1:p.Asn1025Ser
NM_017519.3:c.3074A>G	NP_059989.3:p.Asn1025Ser