Canonical Allele Identifier: CA366234254

Gene: ARID1B

Linked Data

• dbSNP Id: rs1166556361
• gnomAD v4: 6-157189758-A-T
• MyVariant Identifiers: chr6:g.157510892A>T (hg19) ; chr6:g.157189758A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189758A>T , CM000668.2:g.157189758A>T	GRCh38
NC_000006.11:g.157510892A>T , CM000668.1:g.157510892A>T	GRCh37
NC_000006.10:g.157552584A>T	NCBI36
NG_032093.1:g.416829A>T
NG_032093.2:g.416829A>T
NG_066624.1:g.418733A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3877A>T	ENSP00000055163.8:p.Met1293Leu
ENST00000414678.8:c.3946A>T	ENSP00000412835.3:p.Met1316Leu
ENST00000637015.2:c.4165A>T	ENSP00000489729.2:p.Met1389Leu
ENST00000346085.10:c.3916A>T	ENSP00000344546.5:p.Met1306Leu
ENST00000350026.10:c.3628A>T	ENSP00000055163.7:p.Met1210Leu
ENST00000414678.7:c.2194A>T	ENSP00000412835.2:p.Met732Leu
ENST00000635849.1:c.1357A>T	ENSP00000490948.1:p.Met453Leu
ENST00000635957.1:c.991A>T	ENSP00000490385.1:p.Met331Leu
ENST00000636930.2:c.4036A>T MANE Select	ENSP00000490491.2:p.Met1346Leu
ENST00000636940.1:n.2033A>T
ENST00000637015.1:c.1404A>T
ENST00000637568.1:c.1318A>T
ENST00000637741.1:n.702A>T
ENST00000637810.1:c.1378A>T	ENSP00000489636.1:p.Met460Leu
ENST00000637904.1:c.1537A>T	ENSP00000490550.1:p.Met513Leu
ENST00000647938.1:c.3667A>T	ENSP00000498155.1:p.Met1223Leu
ENST00000346085.9:c.3667A>T	ENSP00000344546.4:p.Met1223Leu
ENST00000350026.9:c.3628A>T	ENSP00000055163.7:p.Met1210Leu
ENST00000414678.6:c.2194A>T	ENSP00000412835.2:p.Met732Leu
NM_017519.2:c.3628A>T	NP_059989.2:p.Met1210Leu
NM_020732.3:c.3667A>T	NP_065783.3:p.Met1223Leu
XM_005267069.3:c.3787A>T	XP_005267126.2:p.Met1263Leu
XM_011535984.1:c.2866A>T	XP_011534286.1:p.Met956Leu
XM_011535985.1:c.2686A>T	XP_011534287.1:p.Met896Leu
XM_011535986.1:c.2446A>T	XP_011534288.1:p.Met816Leu
XM_011535987.1:c.2065A>T	XP_011534289.1:p.Met689Leu
XM_011535988.1:c.928A>T	XP_011534290.1:p.Met310Leu
NM_001346813.1:c.3787A>T	NP_001333742.1:p.Met1263Leu
NM_001363725.1:c.1537A>T	NP_001350654.1:p.Met513Leu
XM_011535984.2:c.3997A>T	XP_011534286.2:p.Met1333Leu
XM_011535988.3:c.928A>T	XP_011534290.1:p.Met310Leu
XM_017011103.2:c.3898A>T	XP_016866592.1:p.Met1300Leu
XM_017011104.1:c.3868A>T	XP_016866593.1:p.Met1290Leu
XM_017011105.2:c.3838A>T	XP_016866594.1:p.Met1280Leu
XM_017011106.2:c.3709A>T	XP_016866595.1:p.Met1237Leu
XM_017011107.2:c.3688A>T	XP_016866596.1:p.Met1230Leu
XR_002956289.1:n.4080A>T
NM_001363725.2:c.1537A>T	NP_001350654.1:p.Met513Leu
NM_001371656.1:c.3916A>T	NP_001358585.1:p.Met1306Leu
NM_001374820.1:c.3916A>T	NP_001361749.1:p.Met1306Leu
NM_001374828.1:c.4036A>T MANE Select	NP_001361757.1:p.Met1346Leu
NM_017519.3:c.3877A>T	NP_059989.3:p.Met1293Leu