Canonical Allele Identifier: CA366228444

Gene: ARID1B

Linked Data

• dbSNP Id: rs1792495552
• gnomAD v4: 6-157181161-A-T
• MyVariant Identifiers: chr6:g.157502295A>T (hg19) ; chr6:g.157181161A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181161A>T , CM000668.2:g.157181161A>T	GRCh38
NC_000006.11:g.157502295A>T , CM000668.1:g.157502295A>T	GRCh37
NC_000006.10:g.157543987A>T	NCBI36
NG_032093.1:g.408232A>T
NG_032093.2:g.408232A>T
NG_066624.1:g.410136A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3538A>T	ENSP00000055163.8:p.Ile1180Phe
ENST00000414678.8:c.3607A>T	ENSP00000412835.3:p.Ile1203Phe
ENST00000637015.2:c.3826A>T	ENSP00000489729.2:p.Ile1276Phe
ENST00000319584.11:c.1711A>T	ENSP00000313006.7:p.Ile571Phe
ENST00000346085.10:c.3577A>T	ENSP00000344546.5:p.Ile1193Phe
ENST00000350026.10:c.3289A>T	ENSP00000055163.7:p.Ile1097Phe
ENST00000414678.7:c.1855A>T	ENSP00000412835.2:p.Ile619Phe
ENST00000635849.1:c.1018A>T	ENSP00000490948.1:p.Ile340Phe
ENST00000635957.1:c.652A>T	ENSP00000490385.1:p.Ile218Phe
ENST00000636930.2:c.3697A>T MANE Select	ENSP00000490491.2:p.Ile1233Phe
ENST00000636940.1:n.1694A>T
ENST00000637015.1:c.1065A>T
ENST00000637568.1:c.979A>T
ENST00000637741.1:n.363A>T
ENST00000637810.1:c.1039A>T	ENSP00000489636.1:p.Ile347Phe
ENST00000637904.1:c.1198A>T	ENSP00000490550.1:p.Ile400Phe
ENST00000647938.1:c.3328A>T	ENSP00000498155.1:p.Ile1110Phe
ENST00000319584.10:c.1714A>T	ENSP00000313006.6:p.Ile572Phe
ENST00000346085.9:c.3328A>T	ENSP00000344546.4:p.Ile1110Phe
ENST00000350026.9:c.3289A>T	ENSP00000055163.7:p.Ile1097Phe
ENST00000400790.3:c.490A>T	ENSP00000383596.3:p.Ile164Phe
ENST00000414678.6:c.1855A>T	ENSP00000412835.2:p.Ile619Phe
ENST00000478761.3:c.899A>T
NM_017519.2:c.3289A>T	NP_059989.2:p.Ile1097Phe
NM_020732.3:c.3328A>T	NP_065783.3:p.Ile1110Phe
XM_005267069.3:c.3448A>T	XP_005267126.2:p.Ile1150Phe
XM_011535984.1:c.2527A>T	XP_011534286.1:p.Ile843Phe
XM_011535985.1:c.2347A>T	XP_011534287.1:p.Ile783Phe
XM_011535986.1:c.2107A>T	XP_011534288.1:p.Ile703Phe
XM_011535987.1:c.1726A>T	XP_011534289.1:p.Ile576Phe
XM_011535988.1:c.589A>T	XP_011534290.1:p.Ile197Phe
NM_001346813.1:c.3448A>T	NP_001333742.1:p.Ile1150Phe
NM_001363725.1:c.1198A>T	NP_001350654.1:p.Ile400Phe
XM_011535984.2:c.3658A>T	XP_011534286.2:p.Ile1220Phe
XM_011535988.3:c.589A>T	XP_011534290.1:p.Ile197Phe
XM_017011103.2:c.3559A>T	XP_016866592.1:p.Ile1187Phe
XM_017011104.1:c.3529A>T	XP_016866593.1:p.Ile1177Phe
XM_017011105.2:c.3499A>T	XP_016866594.1:p.Ile1167Phe
XM_017011106.2:c.3370A>T	XP_016866595.1:p.Ile1124Phe
XM_017011107.2:c.3349A>T	XP_016866596.1:p.Ile1117Phe
XR_002956289.1:n.3741A>T
NM_001363725.2:c.1198A>T	NP_001350654.1:p.Ile400Phe
NM_001371656.1:c.3577A>T	NP_001358585.1:p.Ile1193Phe
NM_001374820.1:c.3577A>T	NP_001361749.1:p.Ile1193Phe
NM_001374828.1:c.3697A>T MANE Select	NP_001361757.1:p.Ile1233Phe
NM_017519.3:c.3538A>T	NP_059989.3:p.Ile1180Phe