Canonical Allele Identifier: CA366389275

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470069A>T (hg19) ; chr6:g.157148935A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148935A>T , CM000668.2:g.157148935A>T	GRCh38
NC_000006.11:g.157470069A>T , CM000668.1:g.157470069A>T	GRCh37
NC_000006.10:g.157511761A>T	NCBI36
NG_032093.1:g.376006A>T
NG_032093.2:g.376006A>T
NG_066624.1:g.377910A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3073A>T	ENSP00000055163.8:p.Asn1025Tyr
ENST00000414678.8:c.2983A>T	ENSP00000412835.3:p.Asn995Tyr
ENST00000637015.2:c.3073A>T	ENSP00000489729.2:p.Asn1025Tyr
ENST00000319584.11:c.1087A>T	ENSP00000313006.7:p.Asn363Tyr
ENST00000346085.10:c.3112A>T	ENSP00000344546.5:p.Asn1038Tyr
ENST00000350026.10:c.2824A>T	ENSP00000055163.7:p.Asn942Tyr
ENST00000414678.7:c.1231A>T	ENSP00000412835.2:p.Asn411Tyr
ENST00000452544.2:n.974A>T
ENST00000635849.1:c.394A>T	ENSP00000490948.1:p.Asn132Tyr
ENST00000635957.1:c.28A>T	ENSP00000490385.1:p.Asn10Tyr
ENST00000636426.1:n.207A>T
ENST00000636930.2:c.3073A>T MANE Select	ENSP00000490491.2:p.Asn1025Tyr
ENST00000637015.1:c.312A>T
ENST00000637568.1:c.116A>T
ENST00000637810.1:c.574A>T	ENSP00000489636.1:p.Asn192Tyr
ENST00000637904.1:c.574A>T	ENSP00000490550.1:p.Asn192Tyr
ENST00000647938.1:c.2863A>T	ENSP00000498155.1:p.Asn955Tyr
ENST00000674190.1:n.1822A>T
ENST00000319584.10:c.1090A>T	ENSP00000313006.6:p.Asn364Tyr
ENST00000346085.9:c.2863A>T	ENSP00000344546.4:p.Asn955Tyr
ENST00000350026.9:c.2824A>T	ENSP00000055163.7:p.Asn942Tyr
ENST00000400790.3:c.25A>T	ENSP00000383596.3:p.Asn9Tyr
ENST00000414678.6:c.1231A>T	ENSP00000412835.2:p.Asn411Tyr
ENST00000452544.1:n.920A>T
ENST00000478761.3:c.146A>T
NM_017519.2:c.2824A>T	NP_059989.2:p.Asn942Tyr
NM_020732.3:c.2863A>T	NP_065783.3:p.Asn955Tyr
XM_005267069.3:c.2824A>T	XP_005267126.2:p.Asn942Tyr
XM_011535984.1:c.1774A>T	XP_011534286.1:p.Asn592Tyr
XM_011535985.1:c.1594A>T	XP_011534287.1:p.Asn532Tyr
XM_011535986.1:c.1354A>T	XP_011534288.1:p.Asn452Tyr
XM_011535987.1:c.973A>T	XP_011534289.1:p.Asn325Tyr
XM_011535988.1:c.-20+15728A>T	XP_011534290.1:n.-20+15728A>T
NM_001346813.1:c.2824A>T	NP_001333742.1:p.Asn942Tyr
NM_001363725.1:c.574A>T	NP_001350654.1:p.Asn192Tyr
XM_011535984.2:c.2905A>T	XP_011534286.2:p.Asn969Tyr
XM_011535988.3:c.-20+15728A>T	XP_011534290.1:n.-20+15728A>T
XM_017011103.2:c.2905A>T	XP_016866592.1:p.Asn969Tyr
XM_017011104.1:c.2905A>T	XP_016866593.1:p.Asn969Tyr
XM_017011105.2:c.2905A>T	XP_016866594.1:p.Asn969Tyr
XM_017011106.2:c.2905A>T	XP_016866595.1:p.Asn969Tyr
XM_017011107.2:c.2725A>T	XP_016866596.1:p.Asn909Tyr
XR_002956289.1:n.2988A>T
NM_001363725.2:c.574A>T	NP_001350654.1:p.Asn192Tyr
NM_001371656.1:c.3112A>T	NP_001358585.1:p.Asn1038Tyr
NM_001374820.1:c.3112A>T	NP_001361749.1:p.Asn1038Tyr
NM_001374828.1:c.3073A>T MANE Select	NP_001361757.1:p.Asn1025Tyr
NM_017519.3:c.3073A>T	NP_059989.3:p.Asn1025Tyr