Canonical Allele Identifier: CA366241785

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522199C>G (hg19) ; chr6:g.157201065C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4681C>G	ENSP00000055163.8:p.Pro1561Ala
ENST00000414678.8:c.4750C>G	ENSP00000412835.3:p.Pro1584Ala
ENST00000637015.2:c.4969C>G	ENSP00000489729.2:p.Pro1657Ala
ENST00000346085.10:c.4720C>G	ENSP00000344546.5:p.Pro1574Ala
ENST00000350026.10:c.4432C>G	ENSP00000055163.7:p.Pro1478Ala
ENST00000414678.7:c.2998C>G	ENSP00000412835.2:p.Pro1000Ala
ENST00000635849.1:c.2161C>G	ENSP00000490948.1:p.Pro721Ala
ENST00000635957.1:c.1792C>G	ENSP00000490385.1:p.Pro598Ala
ENST00000636227.1:n.3303C>G
ENST00000636254.1:n.760C>G
ENST00000636930.2:c.4840C>G MANE Select	ENSP00000490491.2:p.Pro1614Ala
ENST00000636940.1:n.2837C>G
ENST00000637015.1:c.2208C>G
ENST00000637568.1:c.2122C>G
ENST00000637741.1:n.1506C>G
ENST00000637810.1:c.2182C>G	ENSP00000489636.1:p.Pro728Ala
ENST00000637904.1:c.2341C>G	ENSP00000490550.1:p.Pro781Ala
ENST00000647938.1:c.4471C>G	ENSP00000498155.1:p.Pro1491Ala
ENST00000346085.9:c.4471C>G	ENSP00000344546.4:p.Pro1491Ala
ENST00000350026.9:c.4432C>G	ENSP00000055163.7:p.Pro1478Ala
ENST00000414678.6:c.2998C>G	ENSP00000412835.2:p.Pro1000Ala
NM_017519.2:c.4432C>G	NP_059989.2:p.Pro1478Ala
NM_020732.3:c.4471C>G	NP_065783.3:p.Pro1491Ala
XM_005267069.3:c.4591C>G	XP_005267126.2:p.Pro1531Ala
XM_011535984.1:c.3670C>G	XP_011534286.1:p.Pro1224Ala
XM_011535985.1:c.3490C>G	XP_011534287.1:p.Pro1164Ala
XM_011535986.1:c.3250C>G	XP_011534288.1:p.Pro1084Ala
XM_011535987.1:c.2869C>G	XP_011534289.1:p.Pro957Ala
XM_011535988.1:c.1732C>G	XP_011534290.1:p.Pro578Ala
NM_001346813.1:c.4591C>G	NP_001333742.1:p.Pro1531Ala
NM_001363725.1:c.2341C>G	NP_001350654.1:p.Pro781Ala
XM_011535984.2:c.4801C>G	XP_011534286.2:p.Pro1601Ala
XM_011535988.3:c.1732C>G	XP_011534290.1:p.Pro578Ala
XM_017011103.2:c.4702C>G	XP_016866592.1:p.Pro1568Ala
XM_017011104.1:c.4672C>G	XP_016866593.1:p.Pro1558Ala
XM_017011105.2:c.4642C>G	XP_016866594.1:p.Pro1548Ala
XM_017011106.2:c.4513C>G	XP_016866595.1:p.Pro1505Ala
XM_017011107.2:c.4492C>G	XP_016866596.1:p.Pro1498Ala
XR_002956289.1:n.4787C>G
NM_001363725.2:c.2341C>G	NP_001350654.1:p.Pro781Ala
NM_001371656.1:c.4720C>G	NP_001358585.1:p.Pro1574Ala
NM_001374820.1:c.4720C>G	NP_001361749.1:p.Pro1574Ala
NM_001374828.1:c.4840C>G MANE Select	NP_001361757.1:p.Pro1614Ala
NM_017519.3:c.4681C>G	NP_059989.3:p.Pro1561Ala