Canonical Allele Identifier: CA366242778

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522502G>T (hg19) ; chr6:g.157201368G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201368G>T , CM000668.2:g.157201368G>T	GRCh38
NC_000006.11:g.157522502G>T , CM000668.1:g.157522502G>T	GRCh37
NC_000006.10:g.157564194G>T	NCBI36
NG_032093.1:g.428439G>T
NG_032093.2:g.428439G>T
NG_066624.1:g.430343G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4984G>T	ENSP00000055163.8:p.Val1662Phe
ENST00000414678.8:c.5053G>T	ENSP00000412835.3:p.Val1685Phe
ENST00000637015.2:c.5272G>T	ENSP00000489729.2:p.Val1758Phe
ENST00000346085.10:c.5023G>T	ENSP00000344546.5:p.Val1675Phe
ENST00000350026.10:c.4735G>T	ENSP00000055163.7:p.Val1579Phe
ENST00000414678.7:c.3301G>T	ENSP00000412835.2:p.Val1101Phe
ENST00000635849.1:c.2464G>T	ENSP00000490948.1:p.Val822Phe
ENST00000635957.1:c.2095G>T	ENSP00000490385.1:p.Val699Phe
ENST00000636227.1:n.3606G>T
ENST00000636254.1:n.1063G>T
ENST00000636930.2:c.5143G>T MANE Select	ENSP00000490491.2:p.Val1715Phe
ENST00000636940.1:n.3140G>T
ENST00000637015.1:c.2511G>T
ENST00000637568.1:c.2425G>T
ENST00000637741.1:n.1809G>T
ENST00000637810.1:c.2485G>T	ENSP00000489636.1:p.Val829Phe
ENST00000637904.1:c.2644G>T	ENSP00000490550.1:p.Val882Phe
ENST00000647938.1:c.4774G>T	ENSP00000498155.1:p.Val1592Phe
ENST00000346085.9:c.4774G>T	ENSP00000344546.4:p.Val1592Phe
ENST00000350026.9:c.4735G>T	ENSP00000055163.7:p.Val1579Phe
ENST00000414678.6:c.3301G>T	ENSP00000412835.2:p.Val1101Phe
NM_017519.2:c.4735G>T	NP_059989.2:p.Val1579Phe
NM_020732.3:c.4774G>T	NP_065783.3:p.Val1592Phe
XM_005267069.3:c.4894G>T	XP_005267126.2:p.Val1632Phe
XM_011535984.1:c.3973G>T	XP_011534286.1:p.Val1325Phe
XM_011535985.1:c.3793G>T	XP_011534287.1:p.Val1265Phe
XM_011535986.1:c.3553G>T	XP_011534288.1:p.Val1185Phe
XM_011535987.1:c.3172G>T	XP_011534289.1:p.Val1058Phe
XM_011535988.1:c.2035G>T	XP_011534290.1:p.Val679Phe
NM_001346813.1:c.4894G>T	NP_001333742.1:p.Val1632Phe
NM_001363725.1:c.2644G>T	NP_001350654.1:p.Val882Phe
XM_011535984.2:c.5104G>T	XP_011534286.2:p.Val1702Phe
XM_011535988.3:c.2035G>T	XP_011534290.1:p.Val679Phe
XM_017011103.2:c.5005G>T	XP_016866592.1:p.Val1669Phe
XM_017011104.1:c.4975G>T	XP_016866593.1:p.Val1659Phe
XM_017011105.2:c.4945G>T	XP_016866594.1:p.Val1649Phe
XM_017011106.2:c.4816G>T	XP_016866595.1:p.Val1606Phe
XM_017011107.2:c.4795G>T	XP_016866596.1:p.Val1599Phe
XR_002956289.1:n.5090G>T
NM_001363725.2:c.2644G>T	NP_001350654.1:p.Val882Phe
NM_001371656.1:c.5023G>T	NP_001358585.1:p.Val1675Phe
NM_001374820.1:c.5023G>T	NP_001361749.1:p.Val1675Phe
NM_001374828.1:c.5143G>T MANE Select	NP_001361757.1:p.Val1715Phe
NM_017519.3:c.4984G>T	NP_059989.3:p.Val1662Phe