Canonical Allele Identifier: CA366234241

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554232975
• MyVariant Identifiers: chr6:g.157510889C>T (hg19) ; chr6:g.157189755C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189755C>T , CM000668.2:g.157189755C>T	GRCh38
NC_000006.11:g.157510889C>T , CM000668.1:g.157510889C>T	GRCh37
NC_000006.10:g.157552581C>T	NCBI36
NG_032093.1:g.416826C>T
NG_032093.2:g.416826C>T
NG_066624.1:g.418730C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3874C>T	ENSP00000055163.8:p.Gln1292Ter
ENST00000414678.8:c.3943C>T	ENSP00000412835.3:p.Gln1315Ter
ENST00000637015.2:c.4162C>T	ENSP00000489729.2:p.Gln1388Ter
ENST00000346085.10:c.3913C>T	ENSP00000344546.5:p.Gln1305Ter
ENST00000350026.10:c.3625C>T	ENSP00000055163.7:p.Gln1209Ter
ENST00000414678.7:c.2191C>T	ENSP00000412835.2:p.Gln731Ter
ENST00000635849.1:c.1354C>T	ENSP00000490948.1:p.Gln452Ter
ENST00000635957.1:c.988C>T	ENSP00000490385.1:p.Gln330Ter
ENST00000636930.2:c.4033C>T MANE Select	ENSP00000490491.2:p.Gln1345Ter
ENST00000636940.1:n.2030C>T
ENST00000637015.1:c.1401C>T
ENST00000637568.1:c.1315C>T
ENST00000637741.1:n.699C>T
ENST00000637810.1:c.1375C>T	ENSP00000489636.1:p.Gln459Ter
ENST00000637904.1:c.1534C>T	ENSP00000490550.1:p.Gln512Ter
ENST00000647938.1:c.3664C>T	ENSP00000498155.1:p.Gln1222Ter
ENST00000346085.9:c.3664C>T	ENSP00000344546.4:p.Gln1222Ter
ENST00000350026.9:c.3625C>T	ENSP00000055163.7:p.Gln1209Ter
ENST00000414678.6:c.2191C>T	ENSP00000412835.2:p.Gln731Ter
NM_017519.2:c.3625C>T	NP_059989.2:p.Gln1209Ter
NM_020732.3:c.3664C>T	NP_065783.3:p.Gln1222Ter
XM_005267069.3:c.3784C>T	XP_005267126.2:p.Gln1262Ter
XM_011535984.1:c.2863C>T	XP_011534286.1:p.Gln955Ter
XM_011535985.1:c.2683C>T	XP_011534287.1:p.Gln895Ter
XM_011535986.1:c.2443C>T	XP_011534288.1:p.Gln815Ter
XM_011535987.1:c.2062C>T	XP_011534289.1:p.Gln688Ter
XM_011535988.1:c.925C>T	XP_011534290.1:p.Gln309Ter
NM_001346813.1:c.3784C>T	NP_001333742.1:p.Gln1262Ter
NM_001363725.1:c.1534C>T	NP_001350654.1:p.Gln512Ter
XM_011535984.2:c.3994C>T	XP_011534286.2:p.Gln1332Ter
XM_011535988.3:c.925C>T	XP_011534290.1:p.Gln309Ter
XM_017011103.2:c.3895C>T	XP_016866592.1:p.Gln1299Ter
XM_017011104.1:c.3865C>T	XP_016866593.1:p.Gln1289Ter
XM_017011105.2:c.3835C>T	XP_016866594.1:p.Gln1279Ter
XM_017011106.2:c.3706C>T	XP_016866595.1:p.Gln1236Ter
XM_017011107.2:c.3685C>T	XP_016866596.1:p.Gln1229Ter
XR_002956289.1:n.4077C>T
NM_001363725.2:c.1534C>T	NP_001350654.1:p.Gln512Ter
NM_001371656.1:c.3913C>T	NP_001358585.1:p.Gln1305Ter
NM_001374820.1:c.3913C>T	NP_001361749.1:p.Gln1305Ter
NM_001374828.1:c.4033C>T MANE Select	NP_001361757.1:p.Gln1345Ter
NM_017519.3:c.3874C>T	NP_059989.3:p.Gln1292Ter