Canonical Allele Identifier: CA366242433

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522431C>T (hg19) ; chr6:g.157201297C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201297C>T , CM000668.2:g.157201297C>T	GRCh38
NC_000006.11:g.157522431C>T , CM000668.1:g.157522431C>T	GRCh37
NC_000006.10:g.157564123C>T	NCBI36
NG_032093.1:g.428368C>T
NG_032093.2:g.428368C>T
NG_066624.1:g.430272C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4913C>T	ENSP00000055163.8:p.Ser1638Phe
ENST00000414678.8:c.4982C>T	ENSP00000412835.3:p.Ser1661Phe
ENST00000637015.2:c.5201C>T	ENSP00000489729.2:p.Ser1734Phe
ENST00000346085.10:c.4952C>T	ENSP00000344546.5:p.Ser1651Phe
ENST00000350026.10:c.4664C>T	ENSP00000055163.7:p.Ser1555Phe
ENST00000414678.7:c.3230C>T	ENSP00000412835.2:p.Ser1077Phe
ENST00000635849.1:c.2393C>T	ENSP00000490948.1:p.Ser798Phe
ENST00000635957.1:c.2024C>T	ENSP00000490385.1:p.Ser675Phe
ENST00000636227.1:n.3535C>T
ENST00000636254.1:n.992C>T
ENST00000636930.2:c.5072C>T MANE Select	ENSP00000490491.2:p.Ser1691Phe
ENST00000636940.1:n.3069C>T
ENST00000637015.1:c.2440C>T
ENST00000637568.1:c.2354C>T
ENST00000637741.1:n.1738C>T
ENST00000637810.1:c.2414C>T	ENSP00000489636.1:p.Ser805Phe
ENST00000637904.1:c.2573C>T	ENSP00000490550.1:p.Ser858Phe
ENST00000647938.1:c.4703C>T	ENSP00000498155.1:p.Ser1568Phe
ENST00000346085.9:c.4703C>T	ENSP00000344546.4:p.Ser1568Phe
ENST00000350026.9:c.4664C>T	ENSP00000055163.7:p.Ser1555Phe
ENST00000414678.6:c.3230C>T	ENSP00000412835.2:p.Ser1077Phe
NM_017519.2:c.4664C>T	NP_059989.2:p.Ser1555Phe
NM_020732.3:c.4703C>T	NP_065783.3:p.Ser1568Phe
XM_005267069.3:c.4823C>T	XP_005267126.2:p.Ser1608Phe
XM_011535984.1:c.3902C>T	XP_011534286.1:p.Ser1301Phe
XM_011535985.1:c.3722C>T	XP_011534287.1:p.Ser1241Phe
XM_011535986.1:c.3482C>T	XP_011534288.1:p.Ser1161Phe
XM_011535987.1:c.3101C>T	XP_011534289.1:p.Ser1034Phe
XM_011535988.1:c.1964C>T	XP_011534290.1:p.Ser655Phe
NM_001346813.1:c.4823C>T	NP_001333742.1:p.Ser1608Phe
NM_001363725.1:c.2573C>T	NP_001350654.1:p.Ser858Phe
XM_011535984.2:c.5033C>T	XP_011534286.2:p.Ser1678Phe
XM_011535988.3:c.1964C>T	XP_011534290.1:p.Ser655Phe
XM_017011103.2:c.4934C>T	XP_016866592.1:p.Ser1645Phe
XM_017011104.1:c.4904C>T	XP_016866593.1:p.Ser1635Phe
XM_017011105.2:c.4874C>T	XP_016866594.1:p.Ser1625Phe
XM_017011106.2:c.4745C>T	XP_016866595.1:p.Ser1582Phe
XM_017011107.2:c.4724C>T	XP_016866596.1:p.Ser1575Phe
XR_002956289.1:n.5019C>T
NM_001363725.2:c.2573C>T	NP_001350654.1:p.Ser858Phe
NM_001371656.1:c.4952C>T	NP_001358585.1:p.Ser1651Phe
NM_001374820.1:c.4952C>T	NP_001361749.1:p.Ser1651Phe
NM_001374828.1:c.5072C>T MANE Select	NP_001361757.1:p.Ser1691Phe
NM_017519.3:c.4913C>T	NP_059989.3:p.Ser1638Phe