Canonical Allele Identifier: CA366388642

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469778G>A (hg19) ; chr6:g.157148644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148644G>A , CM000668.2:g.157148644G>A	GRCh38
NC_000006.11:g.157469778G>A , CM000668.1:g.157469778G>A	GRCh37
NC_000006.10:g.157511470G>A	NCBI36
NG_032093.1:g.375715G>A
NG_032093.2:g.375715G>A
NG_066624.1:g.377619G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2782G>A	ENSP00000055163.8:p.Ala928Thr
ENST00000414678.8:c.2692G>A	ENSP00000412835.3:p.Ala898Thr
ENST00000637015.2:c.2782G>A	ENSP00000489729.2:p.Ala928Thr
ENST00000319584.11:c.796G>A	ENSP00000313006.7:p.Ala266Thr
ENST00000346085.10:c.2821G>A	ENSP00000344546.5:p.Ala941Thr
ENST00000350026.10:c.2533G>A	ENSP00000055163.7:p.Ala845Thr
ENST00000414678.7:c.940G>A	ENSP00000412835.2:p.Ala314Thr
ENST00000452544.2:n.683G>A
ENST00000635849.1:c.103G>A	ENSP00000490948.1:p.Ala35Thr
ENST00000636930.2:c.2782G>A MANE Select	ENSP00000490491.2:p.Ala928Thr
ENST00000637015.1:c.21G>A
ENST00000637810.1:c.283G>A	ENSP00000489636.1:p.Ala95Thr
ENST00000637904.1:c.283G>A	ENSP00000490550.1:p.Ala95Thr
ENST00000647938.1:c.2572G>A	ENSP00000498155.1:p.Ala858Thr
ENST00000674190.1:n.1531G>A
ENST00000319584.10:c.799G>A	ENSP00000313006.6:p.Ala267Thr
ENST00000346085.9:c.2572G>A	ENSP00000344546.4:p.Ala858Thr
ENST00000350026.9:c.2533G>A	ENSP00000055163.7:p.Ala845Thr
ENST00000414678.6:c.940G>A	ENSP00000412835.2:p.Ala314Thr
ENST00000452544.1:n.629G>A
NM_017519.2:c.2533G>A	NP_059989.2:p.Ala845Thr
NM_020732.3:c.2572G>A	NP_065783.3:p.Ala858Thr
XM_005267069.3:c.2533G>A	XP_005267126.2:p.Ala845Thr
XM_011535984.1:c.1483G>A	XP_011534286.1:p.Ala495Thr
XM_011535985.1:c.1303G>A	XP_011534287.1:p.Ala435Thr
XM_011535986.1:c.1063G>A	XP_011534288.1:p.Ala355Thr
XM_011535987.1:c.682G>A	XP_011534289.1:p.Ala228Thr
XM_011535988.1:c.-20+15437G>A	XP_011534290.1:n.-20+15437G>A
NM_001346813.1:c.2533G>A	NP_001333742.1:p.Ala845Thr
NM_001363725.1:c.283G>A	NP_001350654.1:p.Ala95Thr
XM_011535984.2:c.2614G>A	XP_011534286.2:p.Ala872Thr
XM_011535988.3:c.-20+15437G>A	XP_011534290.1:n.-20+15437G>A
XM_017011103.2:c.2614G>A	XP_016866592.1:p.Ala872Thr
XM_017011104.1:c.2614G>A	XP_016866593.1:p.Ala872Thr
XM_017011105.2:c.2614G>A	XP_016866594.1:p.Ala872Thr
XM_017011106.2:c.2614G>A	XP_016866595.1:p.Ala872Thr
XM_017011107.2:c.2434G>A	XP_016866596.1:p.Ala812Thr
XR_002956289.1:n.2697G>A
NM_001363725.2:c.283G>A	NP_001350654.1:p.Ala95Thr
NM_001371656.1:c.2821G>A	NP_001358585.1:p.Ala941Thr
NM_001374820.1:c.2821G>A	NP_001361749.1:p.Ala941Thr
NM_001374828.1:c.2782G>A MANE Select	NP_001361757.1:p.Ala928Thr
NM_017519.3:c.2782G>A	NP_059989.3:p.Ala928Thr