Canonical Allele Identifier: CA366241184

Gene: ARID1B

Linked Data

• dbSNP Id: rs1453652388
• gnomAD v2: 6-157522032-C-T
• gnomAD v3: 6-157200898-C-T
• gnomAD v4: 6-157200898-C-T
• COSMIC: COSM1183556 ; COSM1183557
• MyVariant Identifiers: chr6:g.157522032C>T (hg19) ; chr6:g.157200898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200898C>T , CM000668.2:g.157200898C>T	GRCh38
NC_000006.11:g.157522032C>T , CM000668.1:g.157522032C>T	GRCh37
NC_000006.10:g.157563724C>T	NCBI36
NG_032093.1:g.427969C>T
NG_032093.2:g.427969C>T
NG_066624.1:g.429873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4514C>T	ENSP00000055163.8:p.Pro1505Leu
ENST00000414678.8:c.4583C>T	ENSP00000412835.3:p.Pro1528Leu
ENST00000637015.2:c.4802C>T	ENSP00000489729.2:p.Pro1601Leu
ENST00000346085.10:c.4553C>T	ENSP00000344546.5:p.Pro1518Leu
ENST00000350026.10:c.4265C>T	ENSP00000055163.7:p.Pro1422Leu
ENST00000414678.7:c.2831C>T	ENSP00000412835.2:p.Pro944Leu
ENST00000635849.1:c.1994C>T	ENSP00000490948.1:p.Pro665Leu
ENST00000635957.1:c.1625C>T	ENSP00000490385.1:p.Pro542Leu
ENST00000636227.1:n.3136C>T
ENST00000636254.1:n.593C>T
ENST00000636930.2:c.4673C>T MANE Select	ENSP00000490491.2:p.Pro1558Leu
ENST00000636940.1:n.2670C>T
ENST00000637015.1:c.2041C>T
ENST00000637568.1:c.1955C>T
ENST00000637741.1:n.1339C>T
ENST00000637810.1:c.2015C>T	ENSP00000489636.1:p.Pro672Leu
ENST00000637904.1:c.2174C>T	ENSP00000490550.1:p.Pro725Leu
ENST00000647938.1:c.4304C>T	ENSP00000498155.1:p.Pro1435Leu
ENST00000346085.9:c.4304C>T	ENSP00000344546.4:p.Pro1435Leu
ENST00000350026.9:c.4265C>T	ENSP00000055163.7:p.Pro1422Leu
ENST00000414678.6:c.2831C>T	ENSP00000412835.2:p.Pro944Leu
NM_017519.2:c.4265C>T	NP_059989.2:p.Pro1422Leu
NM_020732.3:c.4304C>T	NP_065783.3:p.Pro1435Leu
XM_005267069.3:c.4424C>T	XP_005267126.2:p.Pro1475Leu
XM_011535984.1:c.3503C>T	XP_011534286.1:p.Pro1168Leu
XM_011535985.1:c.3323C>T	XP_011534287.1:p.Pro1108Leu
XM_011535986.1:c.3083C>T	XP_011534288.1:p.Pro1028Leu
XM_011535987.1:c.2702C>T	XP_011534289.1:p.Pro901Leu
XM_011535988.1:c.1565C>T	XP_011534290.1:p.Pro522Leu
NM_001346813.1:c.4424C>T	NP_001333742.1:p.Pro1475Leu
NM_001363725.1:c.2174C>T	NP_001350654.1:p.Pro725Leu
XM_011535984.2:c.4634C>T	XP_011534286.2:p.Pro1545Leu
XM_011535988.3:c.1565C>T	XP_011534290.1:p.Pro522Leu
XM_017011103.2:c.4535C>T	XP_016866592.1:p.Pro1512Leu
XM_017011104.1:c.4505C>T	XP_016866593.1:p.Pro1502Leu
XM_017011105.2:c.4475C>T	XP_016866594.1:p.Pro1492Leu
XM_017011106.2:c.4346C>T	XP_016866595.1:p.Pro1449Leu
XM_017011107.2:c.4325C>T	XP_016866596.1:p.Pro1442Leu
XR_002956289.1:n.4620C>T
NM_001363725.2:c.2174C>T	NP_001350654.1:p.Pro725Leu
NM_001371656.1:c.4553C>T	NP_001358585.1:p.Pro1518Leu
NM_001374820.1:c.4553C>T	NP_001361749.1:p.Pro1518Leu
NM_001374828.1:c.4673C>T MANE Select	NP_001361757.1:p.Pro1558Leu
NM_017519.3:c.4514C>T	NP_059989.3:p.Pro1505Leu