Canonical Allele Identifier: CA366242005

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235817
• gnomAD v4: 6-157201104-C-G
• MyVariant Identifiers: chr6:g.157522238C>G (hg19) ; chr6:g.157201104C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4720C>G	ENSP00000055163.8:p.Gln1574Glu
ENST00000414678.8:c.4789C>G	ENSP00000412835.3:p.Gln1597Glu
ENST00000637015.2:c.5008C>G	ENSP00000489729.2:p.Gln1670Glu
ENST00000346085.10:c.4759C>G	ENSP00000344546.5:p.Gln1587Glu
ENST00000350026.10:c.4471C>G	ENSP00000055163.7:p.Gln1491Glu
ENST00000414678.7:c.3037C>G	ENSP00000412835.2:p.Gln1013Glu
ENST00000635849.1:c.2200C>G	ENSP00000490948.1:p.Gln734Glu
ENST00000635957.1:c.1831C>G	ENSP00000490385.1:p.Gln611Glu
ENST00000636227.1:n.3342C>G
ENST00000636254.1:n.799C>G
ENST00000636930.2:c.4879C>G MANE Select	ENSP00000490491.2:p.Gln1627Glu
ENST00000636940.1:n.2876C>G
ENST00000637015.1:c.2247C>G
ENST00000637568.1:c.2161C>G
ENST00000637741.1:n.1545C>G
ENST00000637810.1:c.2221C>G	ENSP00000489636.1:p.Gln741Glu
ENST00000637904.1:c.2380C>G	ENSP00000490550.1:p.Gln794Glu
ENST00000647938.1:c.4510C>G	ENSP00000498155.1:p.Gln1504Glu
ENST00000346085.9:c.4510C>G	ENSP00000344546.4:p.Gln1504Glu
ENST00000350026.9:c.4471C>G	ENSP00000055163.7:p.Gln1491Glu
ENST00000414678.6:c.3037C>G	ENSP00000412835.2:p.Gln1013Glu
NM_017519.2:c.4471C>G	NP_059989.2:p.Gln1491Glu
NM_020732.3:c.4510C>G	NP_065783.3:p.Gln1504Glu
XM_005267069.3:c.4630C>G	XP_005267126.2:p.Gln1544Glu
XM_011535984.1:c.3709C>G	XP_011534286.1:p.Gln1237Glu
XM_011535985.1:c.3529C>G	XP_011534287.1:p.Gln1177Glu
XM_011535986.1:c.3289C>G	XP_011534288.1:p.Gln1097Glu
XM_011535987.1:c.2908C>G	XP_011534289.1:p.Gln970Glu
XM_011535988.1:c.1771C>G	XP_011534290.1:p.Gln591Glu
NM_001346813.1:c.4630C>G	NP_001333742.1:p.Gln1544Glu
NM_001363725.1:c.2380C>G	NP_001350654.1:p.Gln794Glu
XM_011535984.2:c.4840C>G	XP_011534286.2:p.Gln1614Glu
XM_011535988.3:c.1771C>G	XP_011534290.1:p.Gln591Glu
XM_017011103.2:c.4741C>G	XP_016866592.1:p.Gln1581Glu
XM_017011104.1:c.4711C>G	XP_016866593.1:p.Gln1571Glu
XM_017011105.2:c.4681C>G	XP_016866594.1:p.Gln1561Glu
XM_017011106.2:c.4552C>G	XP_016866595.1:p.Gln1518Glu
XM_017011107.2:c.4531C>G	XP_016866596.1:p.Gln1511Glu
XR_002956289.1:n.4826C>G
NM_001363725.2:c.2380C>G	NP_001350654.1:p.Gln794Glu
NM_001371656.1:c.4759C>G	NP_001358585.1:p.Gln1587Glu
NM_001374820.1:c.4759C>G	NP_001361749.1:p.Gln1587Glu
NM_001374828.1:c.4879C>G MANE Select	NP_001361757.1:p.Gln1627Glu
NM_017519.3:c.4720C>G	NP_059989.3:p.Gln1574Glu