Canonical Allele Identifier: CA366389161

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470015A>T (hg19) ; chr6:g.157148881A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148881A>T , CM000668.2:g.157148881A>T	GRCh38
NC_000006.11:g.157470015A>T , CM000668.1:g.157470015A>T	GRCh37
NC_000006.10:g.157511707A>T	NCBI36
NG_032093.1:g.375952A>T
NG_032093.2:g.375952A>T
NG_066624.1:g.377856A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3019A>T	ENSP00000055163.8:p.Thr1007Ser
ENST00000414678.8:c.2929A>T	ENSP00000412835.3:p.Thr977Ser
ENST00000637015.2:c.3019A>T	ENSP00000489729.2:p.Thr1007Ser
ENST00000319584.11:c.1033A>T	ENSP00000313006.7:p.Thr345Ser
ENST00000346085.10:c.3058A>T	ENSP00000344546.5:p.Thr1020Ser
ENST00000350026.10:c.2770A>T	ENSP00000055163.7:p.Thr924Ser
ENST00000414678.7:c.1177A>T	ENSP00000412835.2:p.Thr393Ser
ENST00000452544.2:n.920A>T
ENST00000635849.1:c.340A>T	ENSP00000490948.1:p.Thr114Ser
ENST00000636426.1:n.153A>T
ENST00000636930.2:c.3019A>T MANE Select	ENSP00000490491.2:p.Thr1007Ser
ENST00000637015.1:c.258A>T
ENST00000637568.1:c.62A>T
ENST00000637810.1:c.520A>T	ENSP00000489636.1:p.Thr174Ser
ENST00000637904.1:c.520A>T	ENSP00000490550.1:p.Thr174Ser
ENST00000647938.1:c.2809A>T	ENSP00000498155.1:p.Thr937Ser
ENST00000674190.1:n.1768A>T
ENST00000319584.10:c.1036A>T	ENSP00000313006.6:p.Thr346Ser
ENST00000346085.9:c.2809A>T	ENSP00000344546.4:p.Thr937Ser
ENST00000350026.9:c.2770A>T	ENSP00000055163.7:p.Thr924Ser
ENST00000414678.6:c.1177A>T	ENSP00000412835.2:p.Thr393Ser
ENST00000452544.1:n.866A>T
ENST00000478761.3:c.92A>T
NM_017519.2:c.2770A>T	NP_059989.2:p.Thr924Ser
NM_020732.3:c.2809A>T	NP_065783.3:p.Thr937Ser
XM_005267069.3:c.2770A>T	XP_005267126.2:p.Thr924Ser
XM_011535984.1:c.1720A>T	XP_011534286.1:p.Thr574Ser
XM_011535985.1:c.1540A>T	XP_011534287.1:p.Thr514Ser
XM_011535986.1:c.1300A>T	XP_011534288.1:p.Thr434Ser
XM_011535987.1:c.919A>T	XP_011534289.1:p.Thr307Ser
XM_011535988.1:c.-20+15674A>T	XP_011534290.1:n.-20+15674A>T
NM_001346813.1:c.2770A>T	NP_001333742.1:p.Thr924Ser
NM_001363725.1:c.520A>T	NP_001350654.1:p.Thr174Ser
XM_011535984.2:c.2851A>T	XP_011534286.2:p.Thr951Ser
XM_011535988.3:c.-20+15674A>T	XP_011534290.1:n.-20+15674A>T
XM_017011103.2:c.2851A>T	XP_016866592.1:p.Thr951Ser
XM_017011104.1:c.2851A>T	XP_016866593.1:p.Thr951Ser
XM_017011105.2:c.2851A>T	XP_016866594.1:p.Thr951Ser
XM_017011106.2:c.2851A>T	XP_016866595.1:p.Thr951Ser
XM_017011107.2:c.2671A>T	XP_016866596.1:p.Thr891Ser
XR_002956289.1:n.2934A>T
NM_001363725.2:c.520A>T	NP_001350654.1:p.Thr174Ser
NM_001371656.1:c.3058A>T	NP_001358585.1:p.Thr1020Ser
NM_001374820.1:c.3058A>T	NP_001361749.1:p.Thr1020Ser
NM_001374828.1:c.3019A>T MANE Select	NP_001361757.1:p.Thr1007Ser
NM_017519.3:c.3019A>T	NP_059989.3:p.Thr1007Ser