Canonical Allele Identifier: CA366228410

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502290A>T (hg19) ; chr6:g.157181156A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3533A>T	ENSP00000055163.8:p.Lys1178Ile
ENST00000414678.8:c.3602A>T	ENSP00000412835.3:p.Lys1201Ile
ENST00000637015.2:c.3821A>T	ENSP00000489729.2:p.Lys1274Ile
ENST00000319584.11:c.1706A>T	ENSP00000313006.7:p.Lys569Ile
ENST00000346085.10:c.3572A>T	ENSP00000344546.5:p.Lys1191Ile
ENST00000350026.10:c.3284A>T	ENSP00000055163.7:p.Lys1095Ile
ENST00000414678.7:c.1850A>T	ENSP00000412835.2:p.Lys617Ile
ENST00000635849.1:c.1013A>T	ENSP00000490948.1:p.Lys338Ile
ENST00000635957.1:c.647A>T	ENSP00000490385.1:p.Lys216Ile
ENST00000636930.2:c.3692A>T MANE Select	ENSP00000490491.2:p.Lys1231Ile
ENST00000636940.1:n.1689A>T
ENST00000637015.1:c.1060A>T
ENST00000637568.1:c.974A>T
ENST00000637741.1:n.358A>T
ENST00000637810.1:c.1034A>T	ENSP00000489636.1:p.Lys345Ile
ENST00000637904.1:c.1193A>T	ENSP00000490550.1:p.Lys398Ile
ENST00000647938.1:c.3323A>T	ENSP00000498155.1:p.Lys1108Ile
ENST00000319584.10:c.1709A>T	ENSP00000313006.6:p.Lys570Ile
ENST00000346085.9:c.3323A>T	ENSP00000344546.4:p.Lys1108Ile
ENST00000350026.9:c.3284A>T	ENSP00000055163.7:p.Lys1095Ile
ENST00000400790.3:c.485A>T	ENSP00000383596.3:p.Lys162Ile
ENST00000414678.6:c.1850A>T	ENSP00000412835.2:p.Lys617Ile
ENST00000478761.3:c.894A>T
NM_017519.2:c.3284A>T	NP_059989.2:p.Lys1095Ile
NM_020732.3:c.3323A>T	NP_065783.3:p.Lys1108Ile
XM_005267069.3:c.3443A>T	XP_005267126.2:p.Lys1148Ile
XM_011535984.1:c.2522A>T	XP_011534286.1:p.Lys841Ile
XM_011535985.1:c.2342A>T	XP_011534287.1:p.Lys781Ile
XM_011535986.1:c.2102A>T	XP_011534288.1:p.Lys701Ile
XM_011535987.1:c.1721A>T	XP_011534289.1:p.Lys574Ile
XM_011535988.1:c.584A>T	XP_011534290.1:p.Lys195Ile
NM_001346813.1:c.3443A>T	NP_001333742.1:p.Lys1148Ile
NM_001363725.1:c.1193A>T	NP_001350654.1:p.Lys398Ile
XM_011535984.2:c.3653A>T	XP_011534286.2:p.Lys1218Ile
XM_011535988.3:c.584A>T	XP_011534290.1:p.Lys195Ile
XM_017011103.2:c.3554A>T	XP_016866592.1:p.Lys1185Ile
XM_017011104.1:c.3524A>T	XP_016866593.1:p.Lys1175Ile
XM_017011105.2:c.3494A>T	XP_016866594.1:p.Lys1165Ile
XM_017011106.2:c.3365A>T	XP_016866595.1:p.Lys1122Ile
XM_017011107.2:c.3344A>T	XP_016866596.1:p.Lys1115Ile
XR_002956289.1:n.3736A>T
NM_001363725.2:c.1193A>T	NP_001350654.1:p.Lys398Ile
NM_001371656.1:c.3572A>T	NP_001358585.1:p.Lys1191Ile
NM_001374820.1:c.3572A>T	NP_001361749.1:p.Lys1191Ile
NM_001374828.1:c.3692A>T MANE Select	NP_001361757.1:p.Lys1231Ile
NM_017519.3:c.3533A>T	NP_059989.3:p.Lys1178Ile