Canonical Allele Identifier: CA4067375

Gene: ARID1B

Linked Data

• dbSNP Id: rs764452515
• ExAC: 6:157502290 A / G
• gnomAD v2: 6-157502290-A-G
• gnomAD v4: 6-157181156-A-G
• MyVariant Identifiers: chr6:g.157502290A>G (hg19) ; chr6:g.157181156A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181156A>G , CM000668.2:g.157181156A>G	GRCh38
NC_000006.11:g.157502290A>G , CM000668.1:g.157502290A>G	GRCh37
NC_000006.10:g.157543982A>G	NCBI36
NG_032093.1:g.408227A>G
NG_032093.2:g.408227A>G
NG_066624.1:g.410131A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3533A>G	ENSP00000055163.8:p.Lys1178Arg
ENST00000414678.8:c.3602A>G	ENSP00000412835.3:p.Lys1201Arg
ENST00000637015.2:c.3821A>G	ENSP00000489729.2:p.Lys1274Arg
ENST00000319584.11:c.1706A>G	ENSP00000313006.7:p.Lys569Arg
ENST00000346085.10:c.3572A>G	ENSP00000344546.5:p.Lys1191Arg
ENST00000350026.10:c.3284A>G	ENSP00000055163.7:p.Lys1095Arg
ENST00000414678.7:c.1850A>G	ENSP00000412835.2:p.Lys617Arg
ENST00000635849.1:c.1013A>G	ENSP00000490948.1:p.Lys338Arg
ENST00000635957.1:c.647A>G	ENSP00000490385.1:p.Lys216Arg
ENST00000636930.2:c.3692A>G MANE Select	ENSP00000490491.2:p.Lys1231Arg
ENST00000636940.1:n.1689A>G
ENST00000637015.1:c.1060A>G
ENST00000637568.1:c.974A>G
ENST00000637741.1:n.358A>G
ENST00000637810.1:c.1034A>G	ENSP00000489636.1:p.Lys345Arg
ENST00000637904.1:c.1193A>G	ENSP00000490550.1:p.Lys398Arg
ENST00000647938.1:c.3323A>G	ENSP00000498155.1:p.Lys1108Arg
ENST00000319584.10:c.1709A>G	ENSP00000313006.6:p.Lys570Arg
ENST00000346085.9:c.3323A>G	ENSP00000344546.4:p.Lys1108Arg
ENST00000350026.9:c.3284A>G	ENSP00000055163.7:p.Lys1095Arg
ENST00000400790.3:c.485A>G	ENSP00000383596.3:p.Lys162Arg
ENST00000414678.6:c.1850A>G	ENSP00000412835.2:p.Lys617Arg
ENST00000478761.3:c.894A>G
NM_017519.2:c.3284A>G	NP_059989.2:p.Lys1095Arg
NM_020732.3:c.3323A>G	NP_065783.3:p.Lys1108Arg
XM_005267069.3:c.3443A>G	XP_005267126.2:p.Lys1148Arg
XM_011535984.1:c.2522A>G	XP_011534286.1:p.Lys841Arg
XM_011535985.1:c.2342A>G	XP_011534287.1:p.Lys781Arg
XM_011535986.1:c.2102A>G	XP_011534288.1:p.Lys701Arg
XM_011535987.1:c.1721A>G	XP_011534289.1:p.Lys574Arg
XM_011535988.1:c.584A>G	XP_011534290.1:p.Lys195Arg
NM_001346813.1:c.3443A>G	NP_001333742.1:p.Lys1148Arg
NM_001363725.1:c.1193A>G	NP_001350654.1:p.Lys398Arg
XM_011535984.2:c.3653A>G	XP_011534286.2:p.Lys1218Arg
XM_011535988.3:c.584A>G	XP_011534290.1:p.Lys195Arg
XM_017011103.2:c.3554A>G	XP_016866592.1:p.Lys1185Arg
XM_017011104.1:c.3524A>G	XP_016866593.1:p.Lys1175Arg
XM_017011105.2:c.3494A>G	XP_016866594.1:p.Lys1165Arg
XM_017011106.2:c.3365A>G	XP_016866595.1:p.Lys1122Arg
XM_017011107.2:c.3344A>G	XP_016866596.1:p.Lys1115Arg
XR_002956289.1:n.3736A>G
NM_001363725.2:c.1193A>G	NP_001350654.1:p.Lys398Arg
NM_001371656.1:c.3572A>G	NP_001358585.1:p.Lys1191Arg
NM_001374820.1:c.3572A>G	NP_001361749.1:p.Lys1191Arg
NM_001374828.1:c.3692A>G MANE Select	NP_001361757.1:p.Lys1231Arg
NM_017519.3:c.3533A>G	NP_059989.3:p.Lys1178Arg