Canonical Allele Identifier: CA366242367

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522401C>T (hg19) ; chr6:g.157201267C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201267C>T , CM000668.2:g.157201267C>T	GRCh38
NC_000006.11:g.157522401C>T , CM000668.1:g.157522401C>T	GRCh37
NC_000006.10:g.157564093C>T	NCBI36
NG_032093.1:g.428338C>T
NG_032093.2:g.428338C>T
NG_066624.1:g.430242C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4883C>T	ENSP00000055163.8:p.Ser1628Phe
ENST00000414678.8:c.4952C>T	ENSP00000412835.3:p.Ser1651Phe
ENST00000637015.2:c.5171C>T	ENSP00000489729.2:p.Ser1724Phe
ENST00000346085.10:c.4922C>T	ENSP00000344546.5:p.Ser1641Phe
ENST00000350026.10:c.4634C>T	ENSP00000055163.7:p.Ser1545Phe
ENST00000414678.7:c.3200C>T	ENSP00000412835.2:p.Ser1067Phe
ENST00000635849.1:c.2363C>T	ENSP00000490948.1:p.Ser788Phe
ENST00000635957.1:c.1994C>T	ENSP00000490385.1:p.Ser665Phe
ENST00000636227.1:n.3505C>T
ENST00000636254.1:n.962C>T
ENST00000636930.2:c.5042C>T MANE Select	ENSP00000490491.2:p.Ser1681Phe
ENST00000636940.1:n.3039C>T
ENST00000637015.1:c.2410C>T
ENST00000637568.1:c.2324C>T
ENST00000637741.1:n.1708C>T
ENST00000637810.1:c.2384C>T	ENSP00000489636.1:p.Ser795Phe
ENST00000637904.1:c.2543C>T	ENSP00000490550.1:p.Ser848Phe
ENST00000647938.1:c.4673C>T	ENSP00000498155.1:p.Ser1558Phe
ENST00000346085.9:c.4673C>T	ENSP00000344546.4:p.Ser1558Phe
ENST00000350026.9:c.4634C>T	ENSP00000055163.7:p.Ser1545Phe
ENST00000414678.6:c.3200C>T	ENSP00000412835.2:p.Ser1067Phe
NM_017519.2:c.4634C>T	NP_059989.2:p.Ser1545Phe
NM_020732.3:c.4673C>T	NP_065783.3:p.Ser1558Phe
XM_005267069.3:c.4793C>T	XP_005267126.2:p.Ser1598Phe
XM_011535984.1:c.3872C>T	XP_011534286.1:p.Ser1291Phe
XM_011535985.1:c.3692C>T	XP_011534287.1:p.Ser1231Phe
XM_011535986.1:c.3452C>T	XP_011534288.1:p.Ser1151Phe
XM_011535987.1:c.3071C>T	XP_011534289.1:p.Ser1024Phe
XM_011535988.1:c.1934C>T	XP_011534290.1:p.Ser645Phe
NM_001346813.1:c.4793C>T	NP_001333742.1:p.Ser1598Phe
NM_001363725.1:c.2543C>T	NP_001350654.1:p.Ser848Phe
XM_011535984.2:c.5003C>T	XP_011534286.2:p.Ser1668Phe
XM_011535988.3:c.1934C>T	XP_011534290.1:p.Ser645Phe
XM_017011103.2:c.4904C>T	XP_016866592.1:p.Ser1635Phe
XM_017011104.1:c.4874C>T	XP_016866593.1:p.Ser1625Phe
XM_017011105.2:c.4844C>T	XP_016866594.1:p.Ser1615Phe
XM_017011106.2:c.4715C>T	XP_016866595.1:p.Ser1572Phe
XM_017011107.2:c.4694C>T	XP_016866596.1:p.Ser1565Phe
XR_002956289.1:n.4989C>T
NM_001363725.2:c.2543C>T	NP_001350654.1:p.Ser848Phe
NM_001371656.1:c.4922C>T	NP_001358585.1:p.Ser1641Phe
NM_001374820.1:c.4922C>T	NP_001361749.1:p.Ser1641Phe
NM_001374828.1:c.5042C>T MANE Select	NP_001361757.1:p.Ser1681Phe
NM_017519.3:c.4883C>T	NP_059989.3:p.Ser1628Phe