Canonical Allele Identifier: CA366234076

Gene: ARID1B

Linked Data

• dbSNP Id: rs1202710670
• gnomAD v2: 6-157510815-C-T
• gnomAD v4: 6-157189681-C-T
• MyVariant Identifiers: chr6:g.157510815C>T (hg19) ; chr6:g.157189681C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189681C>T , CM000668.2:g.157189681C>T	GRCh38
NC_000006.11:g.157510815C>T , CM000668.1:g.157510815C>T	GRCh37
NC_000006.10:g.157552507C>T	NCBI36
NG_032093.1:g.416752C>T
NG_032093.2:g.416752C>T
NG_066624.1:g.418656C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3800C>T	ENSP00000055163.8:p.Ser1267Leu
ENST00000414678.8:c.3869C>T	ENSP00000412835.3:p.Ser1290Leu
ENST00000637015.2:c.4088C>T	ENSP00000489729.2:p.Ser1363Leu
ENST00000346085.10:c.3839C>T	ENSP00000344546.5:p.Ser1280Leu
ENST00000350026.10:c.3551C>T	ENSP00000055163.7:p.Ser1184Leu
ENST00000414678.7:c.2117C>T	ENSP00000412835.2:p.Ser706Leu
ENST00000635849.1:c.1280C>T	ENSP00000490948.1:p.Ser427Leu
ENST00000635957.1:c.914C>T	ENSP00000490385.1:p.Ser305Leu
ENST00000636930.2:c.3959C>T MANE Select	ENSP00000490491.2:p.Ser1320Leu
ENST00000636940.1:n.1956C>T
ENST00000637015.1:c.1327C>T
ENST00000637568.1:c.1241C>T
ENST00000637741.1:n.625C>T
ENST00000637810.1:c.1301C>T	ENSP00000489636.1:p.Ser434Leu
ENST00000637904.1:c.1460C>T	ENSP00000490550.1:p.Ser487Leu
ENST00000647938.1:c.3590C>T	ENSP00000498155.1:p.Ser1197Leu
ENST00000346085.9:c.3590C>T	ENSP00000344546.4:p.Ser1197Leu
ENST00000350026.9:c.3551C>T	ENSP00000055163.7:p.Ser1184Leu
ENST00000414678.6:c.2117C>T	ENSP00000412835.2:p.Ser706Leu
NM_017519.2:c.3551C>T	NP_059989.2:p.Ser1184Leu
NM_020732.3:c.3590C>T	NP_065783.3:p.Ser1197Leu
XM_005267069.3:c.3710C>T	XP_005267126.2:p.Ser1237Leu
XM_011535984.1:c.2789C>T	XP_011534286.1:p.Ser930Leu
XM_011535985.1:c.2609C>T	XP_011534287.1:p.Ser870Leu
XM_011535986.1:c.2369C>T	XP_011534288.1:p.Ser790Leu
XM_011535987.1:c.1988C>T	XP_011534289.1:p.Ser663Leu
XM_011535988.1:c.851C>T	XP_011534290.1:p.Ser284Leu
NM_001346813.1:c.3710C>T	NP_001333742.1:p.Ser1237Leu
NM_001363725.1:c.1460C>T	NP_001350654.1:p.Ser487Leu
XM_011535984.2:c.3920C>T	XP_011534286.2:p.Ser1307Leu
XM_011535988.3:c.851C>T	XP_011534290.1:p.Ser284Leu
XM_017011103.2:c.3821C>T	XP_016866592.1:p.Ser1274Leu
XM_017011104.1:c.3791C>T	XP_016866593.1:p.Ser1264Leu
XM_017011105.2:c.3761C>T	XP_016866594.1:p.Ser1254Leu
XM_017011106.2:c.3632C>T	XP_016866595.1:p.Ser1211Leu
XM_017011107.2:c.3611C>T	XP_016866596.1:p.Ser1204Leu
XR_002956289.1:n.4003C>T
NM_001363725.2:c.1460C>T	NP_001350654.1:p.Ser487Leu
NM_001371656.1:c.3839C>T	NP_001358585.1:p.Ser1280Leu
NM_001374820.1:c.3839C>T	NP_001361749.1:p.Ser1280Leu
NM_001374828.1:c.3959C>T MANE Select	NP_001361757.1:p.Ser1320Leu
NM_017519.3:c.3800C>T	NP_059989.3:p.Ser1267Leu