Canonical Allele Identifier: CA452978291

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522426C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201292C>T , CM000668.2:g.157201292C>T	GRCh38
NC_000006.11:g.157522426C>T , CM000668.1:g.157522426C>T	GRCh37
NC_000006.10:g.157564118C>T	NCBI36
NG_032093.1:g.428363C>T
NG_032093.2:g.428363C>T
NG_066624.1:g.430267C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4908C>T	ENSP00000055163.8:p.Arg1636=
ENST00000414678.8:c.4977C>T	ENSP00000412835.3:p.Arg1659=
ENST00000637015.2:c.5196C>T	ENSP00000489729.2:p.Arg1732=
ENST00000346085.10:c.4947C>T	ENSP00000344546.5:p.Arg1649=
ENST00000350026.10:c.4659C>T	ENSP00000055163.7:p.Arg1553=
ENST00000414678.7:c.3225C>T	ENSP00000412835.2:p.Arg1075=
ENST00000635849.1:c.2388C>T	ENSP00000490948.1:p.Arg796=
ENST00000635957.1:c.2019C>T	ENSP00000490385.1:p.Arg673=
ENST00000636227.1:n.3530C>T
ENST00000636254.1:n.987C>T
ENST00000636930.2:c.5067C>T MANE Select	ENSP00000490491.2:p.Arg1689=
ENST00000636940.1:n.3064C>T
ENST00000637015.1:c.2435C>T
ENST00000637568.1:c.2349C>T
ENST00000637741.1:n.1733C>T
ENST00000637810.1:c.2409C>T	ENSP00000489636.1:p.Arg803=
ENST00000637904.1:c.2568C>T	ENSP00000490550.1:p.Arg856=
ENST00000647938.1:c.4698C>T	ENSP00000498155.1:p.Arg1566=
ENST00000346085.9:c.4698C>T	ENSP00000344546.4:p.Arg1566=
ENST00000350026.9:c.4659C>T	ENSP00000055163.7:p.Arg1553=
ENST00000414678.6:c.3225C>T	ENSP00000412835.2:p.Arg1075=
NM_017519.2:c.4659C>T	NP_059989.2:p.Arg1553=
NM_020732.3:c.4698C>T	NP_065783.3:p.Arg1566=
XM_005267069.3:c.4818C>T	XP_005267126.2:p.Arg1606=
XM_011535984.1:c.3897C>T	XP_011534286.1:p.Arg1299=
XM_011535985.1:c.3717C>T	XP_011534287.1:p.Arg1239=
XM_011535986.1:c.3477C>T	XP_011534288.1:p.Arg1159=
XM_011535987.1:c.3096C>T	XP_011534289.1:p.Arg1032=
XM_011535988.1:c.1959C>T	XP_011534290.1:p.Arg653=
NM_001346813.1:c.4818C>T	NP_001333742.1:p.Arg1606=
NM_001363725.1:c.2568C>T	NP_001350654.1:p.Arg856=
XM_011535984.2:c.5028C>T	XP_011534286.2:p.Arg1676=
XM_011535988.3:c.1959C>T	XP_011534290.1:p.Arg653=
XM_017011103.2:c.4929C>T	XP_016866592.1:p.Arg1643=
XM_017011104.1:c.4899C>T	XP_016866593.1:p.Arg1633=
XM_017011105.2:c.4869C>T	XP_016866594.1:p.Arg1623=
XM_017011106.2:c.4740C>T	XP_016866595.1:p.Arg1580=
XM_017011107.2:c.4719C>T	XP_016866596.1:p.Arg1573=
XR_002956289.1:n.5014C>T
NM_001363725.2:c.2568C>T	NP_001350654.1:p.Arg856=
NM_001371656.1:c.4947C>T	NP_001358585.1:p.Arg1649=
NM_001374820.1:c.4947C>T	NP_001361749.1:p.Arg1649=
NM_001374828.1:c.5067C>T MANE Select	NP_001361757.1:p.Arg1689=
NM_017519.3:c.4908C>T	NP_059989.3:p.Arg1636=