Canonical Allele Identifier: CA366241783

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374311
• MyVariant Identifiers: chr6:g.157522199C>A (hg19) ; chr6:g.157201065C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201065C>A , CM000668.2:g.157201065C>A	GRCh38
NC_000006.11:g.157522199C>A , CM000668.1:g.157522199C>A	GRCh37
NC_000006.10:g.157563891C>A	NCBI36
NG_032093.1:g.428136C>A
NG_032093.2:g.428136C>A
NG_066624.1:g.430040C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4681C>A	ENSP00000055163.8:p.Pro1561Thr
ENST00000414678.8:c.4750C>A	ENSP00000412835.3:p.Pro1584Thr
ENST00000637015.2:c.4969C>A	ENSP00000489729.2:p.Pro1657Thr
ENST00000346085.10:c.4720C>A	ENSP00000344546.5:p.Pro1574Thr
ENST00000350026.10:c.4432C>A	ENSP00000055163.7:p.Pro1478Thr
ENST00000414678.7:c.2998C>A	ENSP00000412835.2:p.Pro1000Thr
ENST00000635849.1:c.2161C>A	ENSP00000490948.1:p.Pro721Thr
ENST00000635957.1:c.1792C>A	ENSP00000490385.1:p.Pro598Thr
ENST00000636227.1:n.3303C>A
ENST00000636254.1:n.760C>A
ENST00000636930.2:c.4840C>A MANE Select	ENSP00000490491.2:p.Pro1614Thr
ENST00000636940.1:n.2837C>A
ENST00000637015.1:c.2208C>A
ENST00000637568.1:c.2122C>A
ENST00000637741.1:n.1506C>A
ENST00000637810.1:c.2182C>A	ENSP00000489636.1:p.Pro728Thr
ENST00000637904.1:c.2341C>A	ENSP00000490550.1:p.Pro781Thr
ENST00000647938.1:c.4471C>A	ENSP00000498155.1:p.Pro1491Thr
ENST00000346085.9:c.4471C>A	ENSP00000344546.4:p.Pro1491Thr
ENST00000350026.9:c.4432C>A	ENSP00000055163.7:p.Pro1478Thr
ENST00000414678.6:c.2998C>A	ENSP00000412835.2:p.Pro1000Thr
NM_017519.2:c.4432C>A	NP_059989.2:p.Pro1478Thr
NM_020732.3:c.4471C>A	NP_065783.3:p.Pro1491Thr
XM_005267069.3:c.4591C>A	XP_005267126.2:p.Pro1531Thr
XM_011535984.1:c.3670C>A	XP_011534286.1:p.Pro1224Thr
XM_011535985.1:c.3490C>A	XP_011534287.1:p.Pro1164Thr
XM_011535986.1:c.3250C>A	XP_011534288.1:p.Pro1084Thr
XM_011535987.1:c.2869C>A	XP_011534289.1:p.Pro957Thr
XM_011535988.1:c.1732C>A	XP_011534290.1:p.Pro578Thr
NM_001346813.1:c.4591C>A	NP_001333742.1:p.Pro1531Thr
NM_001363725.1:c.2341C>A	NP_001350654.1:p.Pro781Thr
XM_011535984.2:c.4801C>A	XP_011534286.2:p.Pro1601Thr
XM_011535988.3:c.1732C>A	XP_011534290.1:p.Pro578Thr
XM_017011103.2:c.4702C>A	XP_016866592.1:p.Pro1568Thr
XM_017011104.1:c.4672C>A	XP_016866593.1:p.Pro1558Thr
XM_017011105.2:c.4642C>A	XP_016866594.1:p.Pro1548Thr
XM_017011106.2:c.4513C>A	XP_016866595.1:p.Pro1505Thr
XM_017011107.2:c.4492C>A	XP_016866596.1:p.Pro1498Thr
XR_002956289.1:n.4787C>A
NM_001363725.2:c.2341C>A	NP_001350654.1:p.Pro781Thr
NM_001371656.1:c.4720C>A	NP_001358585.1:p.Pro1574Thr
NM_001374820.1:c.4720C>A	NP_001361749.1:p.Pro1574Thr
NM_001374828.1:c.4840C>A MANE Select	NP_001361757.1:p.Pro1614Thr
NM_017519.3:c.4681C>A	NP_059989.3:p.Pro1561Thr