Canonical Allele Identifier: CA366242859

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235993
• MyVariant Identifiers: chr6:g.157522520C>T (hg19) ; chr6:g.157201386C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201386C>T , CM000668.2:g.157201386C>T	GRCh38
NC_000006.11:g.157522520C>T , CM000668.1:g.157522520C>T	GRCh37
NC_000006.10:g.157564212C>T	NCBI36
NG_032093.1:g.428457C>T
NG_032093.2:g.428457C>T
NG_066624.1:g.430361C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5002C>T	ENSP00000055163.8:p.Gln1668Ter
ENST00000414678.8:c.5071C>T	ENSP00000412835.3:p.Gln1691Ter
ENST00000637015.2:c.5290C>T	ENSP00000489729.2:p.Gln1764Ter
ENST00000346085.10:c.5041C>T	ENSP00000344546.5:p.Gln1681Ter
ENST00000350026.10:c.4753C>T	ENSP00000055163.7:p.Gln1585Ter
ENST00000414678.7:c.3319C>T	ENSP00000412835.2:p.Gln1107Ter
ENST00000635849.1:c.2482C>T	ENSP00000490948.1:p.Gln828Ter
ENST00000635957.1:c.2113C>T	ENSP00000490385.1:p.Gln705Ter
ENST00000636227.1:n.3624C>T
ENST00000636254.1:n.1081C>T
ENST00000636930.2:c.5161C>T MANE Select	ENSP00000490491.2:p.Gln1721Ter
ENST00000636940.1:n.3158C>T
ENST00000637015.1:c.2529C>T
ENST00000637568.1:c.2443C>T
ENST00000637741.1:n.1827C>T
ENST00000637810.1:c.2503C>T	ENSP00000489636.1:p.Gln835Ter
ENST00000637904.1:c.2662C>T	ENSP00000490550.1:p.Gln888Ter
ENST00000647938.1:c.4792C>T	ENSP00000498155.1:p.Gln1598Ter
ENST00000346085.9:c.4792C>T	ENSP00000344546.4:p.Gln1598Ter
ENST00000350026.9:c.4753C>T	ENSP00000055163.7:p.Gln1585Ter
ENST00000414678.6:c.3319C>T	ENSP00000412835.2:p.Gln1107Ter
NM_017519.2:c.4753C>T	NP_059989.2:p.Gln1585Ter
NM_020732.3:c.4792C>T	NP_065783.3:p.Gln1598Ter
XM_005267069.3:c.4912C>T	XP_005267126.2:p.Gln1638Ter
XM_011535984.1:c.3991C>T	XP_011534286.1:p.Gln1331Ter
XM_011535985.1:c.3811C>T	XP_011534287.1:p.Gln1271Ter
XM_011535986.1:c.3571C>T	XP_011534288.1:p.Gln1191Ter
XM_011535987.1:c.3190C>T	XP_011534289.1:p.Gln1064Ter
XM_011535988.1:c.2053C>T	XP_011534290.1:p.Gln685Ter
NM_001346813.1:c.4912C>T	NP_001333742.1:p.Gln1638Ter
NM_001363725.1:c.2662C>T	NP_001350654.1:p.Gln888Ter
XM_011535984.2:c.5122C>T	XP_011534286.2:p.Gln1708Ter
XM_011535988.3:c.2053C>T	XP_011534290.1:p.Gln685Ter
XM_017011103.2:c.5023C>T	XP_016866592.1:p.Gln1675Ter
XM_017011104.1:c.4993C>T	XP_016866593.1:p.Gln1665Ter
XM_017011105.2:c.4963C>T	XP_016866594.1:p.Gln1655Ter
XM_017011106.2:c.4834C>T	XP_016866595.1:p.Gln1612Ter
XM_017011107.2:c.4813C>T	XP_016866596.1:p.Gln1605Ter
XR_002956289.1:n.5108C>T
NM_001363725.2:c.2662C>T	NP_001350654.1:p.Gln888Ter
NM_001371656.1:c.5041C>T	NP_001358585.1:p.Gln1681Ter
NM_001374820.1:c.5041C>T	NP_001361749.1:p.Gln1681Ter
NM_001374828.1:c.5161C>T MANE Select	NP_001361757.1:p.Gln1721Ter
NM_017519.3:c.5002C>T	NP_059989.3:p.Gln1668Ter