Canonical Allele Identifier: CA366242006

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235817
• MyVariant Identifiers: chr6:g.157522238C>T (hg19) ; chr6:g.157201104C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201104C>T , CM000668.2:g.157201104C>T	GRCh38
NC_000006.11:g.157522238C>T , CM000668.1:g.157522238C>T	GRCh37
NC_000006.10:g.157563930C>T	NCBI36
NG_032093.1:g.428175C>T
NG_032093.2:g.428175C>T
NG_066624.1:g.430079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4720C>T	ENSP00000055163.8:p.Gln1574Ter
ENST00000414678.8:c.4789C>T	ENSP00000412835.3:p.Gln1597Ter
ENST00000637015.2:c.5008C>T	ENSP00000489729.2:p.Gln1670Ter
ENST00000346085.10:c.4759C>T	ENSP00000344546.5:p.Gln1587Ter
ENST00000350026.10:c.4471C>T	ENSP00000055163.7:p.Gln1491Ter
ENST00000414678.7:c.3037C>T	ENSP00000412835.2:p.Gln1013Ter
ENST00000635849.1:c.2200C>T	ENSP00000490948.1:p.Gln734Ter
ENST00000635957.1:c.1831C>T	ENSP00000490385.1:p.Gln611Ter
ENST00000636227.1:n.3342C>T
ENST00000636254.1:n.799C>T
ENST00000636930.2:c.4879C>T MANE Select	ENSP00000490491.2:p.Gln1627Ter
ENST00000636940.1:n.2876C>T
ENST00000637015.1:c.2247C>T
ENST00000637568.1:c.2161C>T
ENST00000637741.1:n.1545C>T
ENST00000637810.1:c.2221C>T	ENSP00000489636.1:p.Gln741Ter
ENST00000637904.1:c.2380C>T	ENSP00000490550.1:p.Gln794Ter
ENST00000647938.1:c.4510C>T	ENSP00000498155.1:p.Gln1504Ter
ENST00000346085.9:c.4510C>T	ENSP00000344546.4:p.Gln1504Ter
ENST00000350026.9:c.4471C>T	ENSP00000055163.7:p.Gln1491Ter
ENST00000414678.6:c.3037C>T	ENSP00000412835.2:p.Gln1013Ter
NM_017519.2:c.4471C>T	NP_059989.2:p.Gln1491Ter
NM_020732.3:c.4510C>T	NP_065783.3:p.Gln1504Ter
XM_005267069.3:c.4630C>T	XP_005267126.2:p.Gln1544Ter
XM_011535984.1:c.3709C>T	XP_011534286.1:p.Gln1237Ter
XM_011535985.1:c.3529C>T	XP_011534287.1:p.Gln1177Ter
XM_011535986.1:c.3289C>T	XP_011534288.1:p.Gln1097Ter
XM_011535987.1:c.2908C>T	XP_011534289.1:p.Gln970Ter
XM_011535988.1:c.1771C>T	XP_011534290.1:p.Gln591Ter
NM_001346813.1:c.4630C>T	NP_001333742.1:p.Gln1544Ter
NM_001363725.1:c.2380C>T	NP_001350654.1:p.Gln794Ter
XM_011535984.2:c.4840C>T	XP_011534286.2:p.Gln1614Ter
XM_011535988.3:c.1771C>T	XP_011534290.1:p.Gln591Ter
XM_017011103.2:c.4741C>T	XP_016866592.1:p.Gln1581Ter
XM_017011104.1:c.4711C>T	XP_016866593.1:p.Gln1571Ter
XM_017011105.2:c.4681C>T	XP_016866594.1:p.Gln1561Ter
XM_017011106.2:c.4552C>T	XP_016866595.1:p.Gln1518Ter
XM_017011107.2:c.4531C>T	XP_016866596.1:p.Gln1511Ter
XR_002956289.1:n.4826C>T
NM_001363725.2:c.2380C>T	NP_001350654.1:p.Gln794Ter
NM_001371656.1:c.4759C>T	NP_001358585.1:p.Gln1587Ter
NM_001374820.1:c.4759C>T	NP_001361749.1:p.Gln1587Ter
NM_001374828.1:c.4879C>T MANE Select	NP_001361757.1:p.Gln1627Ter
NM_017519.3:c.4720C>T	NP_059989.3:p.Gln1574Ter