Canonical Allele Identifier: CA452978060

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522093C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200959C>G , CM000668.2:g.157200959C>G	GRCh38
NC_000006.11:g.157522093C>G , CM000668.1:g.157522093C>G	GRCh37
NC_000006.10:g.157563785C>G	NCBI36
NG_032093.1:g.428030C>G
NG_032093.2:g.428030C>G
NG_066624.1:g.429934C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4575C>G	ENSP00000055163.8:p.Ser1525=
ENST00000414678.8:c.4644C>G	ENSP00000412835.3:p.Ser1548=
ENST00000637015.2:c.4863C>G	ENSP00000489729.2:p.Ser1621=
ENST00000346085.10:c.4614C>G	ENSP00000344546.5:p.Ser1538=
ENST00000350026.10:c.4326C>G	ENSP00000055163.7:p.Ser1442=
ENST00000414678.7:c.2892C>G	ENSP00000412835.2:p.Ser964=
ENST00000635849.1:c.2055C>G	ENSP00000490948.1:p.Ser685=
ENST00000635957.1:c.1686C>G	ENSP00000490385.1:p.Ser562=
ENST00000636227.1:n.3197C>G
ENST00000636254.1:n.654C>G
ENST00000636930.2:c.4734C>G MANE Select	ENSP00000490491.2:p.Ser1578=
ENST00000636940.1:n.2731C>G
ENST00000637015.1:c.2102C>G
ENST00000637568.1:c.2016C>G
ENST00000637741.1:n.1400C>G
ENST00000637810.1:c.2076C>G	ENSP00000489636.1:p.Ser692=
ENST00000637904.1:c.2235C>G	ENSP00000490550.1:p.Ser745=
ENST00000647938.1:c.4365C>G	ENSP00000498155.1:p.Ser1455=
ENST00000346085.9:c.4365C>G	ENSP00000344546.4:p.Ser1455=
ENST00000350026.9:c.4326C>G	ENSP00000055163.7:p.Ser1442=
ENST00000414678.6:c.2892C>G	ENSP00000412835.2:p.Ser964=
NM_017519.2:c.4326C>G	NP_059989.2:p.Ser1442=
NM_020732.3:c.4365C>G	NP_065783.3:p.Ser1455=
XM_005267069.3:c.4485C>G	XP_005267126.2:p.Ser1495=
XM_011535984.1:c.3564C>G	XP_011534286.1:p.Ser1188=
XM_011535985.1:c.3384C>G	XP_011534287.1:p.Ser1128=
XM_011535986.1:c.3144C>G	XP_011534288.1:p.Ser1048=
XM_011535987.1:c.2763C>G	XP_011534289.1:p.Ser921=
XM_011535988.1:c.1626C>G	XP_011534290.1:p.Ser542=
NM_001346813.1:c.4485C>G	NP_001333742.1:p.Ser1495=
NM_001363725.1:c.2235C>G	NP_001350654.1:p.Ser745=
XM_011535984.2:c.4695C>G	XP_011534286.2:p.Ser1565=
XM_011535988.3:c.1626C>G	XP_011534290.1:p.Ser542=
XM_017011103.2:c.4596C>G	XP_016866592.1:p.Ser1532=
XM_017011104.1:c.4566C>G	XP_016866593.1:p.Ser1522=
XM_017011105.2:c.4536C>G	XP_016866594.1:p.Ser1512=
XM_017011106.2:c.4407C>G	XP_016866595.1:p.Ser1469=
XM_017011107.2:c.4386C>G	XP_016866596.1:p.Ser1462=
XR_002956289.1:n.4681C>G
NM_001363725.2:c.2235C>G	NP_001350654.1:p.Ser745=
NM_001371656.1:c.4614C>G	NP_001358585.1:p.Ser1538=
NM_001374820.1:c.4614C>G	NP_001361749.1:p.Ser1538=
NM_001374828.1:c.4734C>G MANE Select	NP_001361757.1:p.Ser1578=
NM_017519.3:c.4575C>G	NP_059989.3:p.Ser1525=