Canonical Allele Identifier: CA4067487

Gene: ARID1B

Linked Data

• dbSNP Id: rs781326777
• ExAC: 6:157510841 G / C
• gnomAD v2: 6-157510841-G-C
• gnomAD v4: 6-157189707-G-C
• MyVariant Identifiers: chr6:g.157510841G>C (hg19) ; chr6:g.157189707G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189707G>C , CM000668.2:g.157189707G>C	GRCh38
NC_000006.11:g.157510841G>C , CM000668.1:g.157510841G>C	GRCh37
NC_000006.10:g.157552533G>C	NCBI36
NG_032093.1:g.416778G>C
NG_032093.2:g.416778G>C
NG_066624.1:g.418682G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3826G>C	ENSP00000055163.8:p.Val1276Leu
ENST00000414678.8:c.3895G>C	ENSP00000412835.3:p.Val1299Leu
ENST00000637015.2:c.4114G>C	ENSP00000489729.2:p.Val1372Leu
ENST00000346085.10:c.3865G>C	ENSP00000344546.5:p.Val1289Leu
ENST00000350026.10:c.3577G>C	ENSP00000055163.7:p.Val1193Leu
ENST00000414678.7:c.2143G>C	ENSP00000412835.2:p.Val715Leu
ENST00000635849.1:c.1306G>C	ENSP00000490948.1:p.Val436Leu
ENST00000635957.1:c.940G>C	ENSP00000490385.1:p.Val314Leu
ENST00000636930.2:c.3985G>C MANE Select	ENSP00000490491.2:p.Val1329Leu
ENST00000636940.1:n.1982G>C
ENST00000637015.1:c.1353G>C
ENST00000637568.1:c.1267G>C
ENST00000637741.1:n.651G>C
ENST00000637810.1:c.1327G>C	ENSP00000489636.1:p.Val443Leu
ENST00000637904.1:c.1486G>C	ENSP00000490550.1:p.Val496Leu
ENST00000647938.1:c.3616G>C	ENSP00000498155.1:p.Val1206Leu
ENST00000346085.9:c.3616G>C	ENSP00000344546.4:p.Val1206Leu
ENST00000350026.9:c.3577G>C	ENSP00000055163.7:p.Val1193Leu
ENST00000414678.6:c.2143G>C	ENSP00000412835.2:p.Val715Leu
NM_017519.2:c.3577G>C	NP_059989.2:p.Val1193Leu
NM_020732.3:c.3616G>C	NP_065783.3:p.Val1206Leu
XM_005267069.3:c.3736G>C	XP_005267126.2:p.Val1246Leu
XM_011535984.1:c.2815G>C	XP_011534286.1:p.Val939Leu
XM_011535985.1:c.2635G>C	XP_011534287.1:p.Val879Leu
XM_011535986.1:c.2395G>C	XP_011534288.1:p.Val799Leu
XM_011535987.1:c.2014G>C	XP_011534289.1:p.Val672Leu
XM_011535988.1:c.877G>C	XP_011534290.1:p.Val293Leu
NM_001346813.1:c.3736G>C	NP_001333742.1:p.Val1246Leu
NM_001363725.1:c.1486G>C	NP_001350654.1:p.Val496Leu
XM_011535984.2:c.3946G>C	XP_011534286.2:p.Val1316Leu
XM_011535988.3:c.877G>C	XP_011534290.1:p.Val293Leu
XM_017011103.2:c.3847G>C	XP_016866592.1:p.Val1283Leu
XM_017011104.1:c.3817G>C	XP_016866593.1:p.Val1273Leu
XM_017011105.2:c.3787G>C	XP_016866594.1:p.Val1263Leu
XM_017011106.2:c.3658G>C	XP_016866595.1:p.Val1220Leu
XM_017011107.2:c.3637G>C	XP_016866596.1:p.Val1213Leu
XR_002956289.1:n.4029G>C
NM_001363725.2:c.1486G>C	NP_001350654.1:p.Val496Leu
NM_001371656.1:c.3865G>C	NP_001358585.1:p.Val1289Leu
NM_001374820.1:c.3865G>C	NP_001361749.1:p.Val1289Leu
NM_001374828.1:c.3985G>C MANE Select	NP_001361757.1:p.Val1329Leu
NM_017519.3:c.3826G>C	NP_059989.3:p.Val1276Leu