Canonical Allele Identifier: CA366241180

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522031C>G (hg19) ; chr6:g.157200897C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200897C>G , CM000668.2:g.157200897C>G	GRCh38
NC_000006.11:g.157522031C>G , CM000668.1:g.157522031C>G	GRCh37
NC_000006.10:g.157563723C>G	NCBI36
NG_032093.1:g.427968C>G
NG_032093.2:g.427968C>G
NG_066624.1:g.429872C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4513C>G	ENSP00000055163.8:p.Pro1505Ala
ENST00000414678.8:c.4582C>G	ENSP00000412835.3:p.Pro1528Ala
ENST00000637015.2:c.4801C>G	ENSP00000489729.2:p.Pro1601Ala
ENST00000346085.10:c.4552C>G	ENSP00000344546.5:p.Pro1518Ala
ENST00000350026.10:c.4264C>G	ENSP00000055163.7:p.Pro1422Ala
ENST00000414678.7:c.2830C>G	ENSP00000412835.2:p.Pro944Ala
ENST00000635849.1:c.1993C>G	ENSP00000490948.1:p.Pro665Ala
ENST00000635957.1:c.1624C>G	ENSP00000490385.1:p.Pro542Ala
ENST00000636227.1:n.3135C>G
ENST00000636254.1:n.592C>G
ENST00000636930.2:c.4672C>G MANE Select	ENSP00000490491.2:p.Pro1558Ala
ENST00000636940.1:n.2669C>G
ENST00000637015.1:c.2040C>G
ENST00000637568.1:c.1954C>G
ENST00000637741.1:n.1338C>G
ENST00000637810.1:c.2014C>G	ENSP00000489636.1:p.Pro672Ala
ENST00000637904.1:c.2173C>G	ENSP00000490550.1:p.Pro725Ala
ENST00000647938.1:c.4303C>G	ENSP00000498155.1:p.Pro1435Ala
ENST00000346085.9:c.4303C>G	ENSP00000344546.4:p.Pro1435Ala
ENST00000350026.9:c.4264C>G	ENSP00000055163.7:p.Pro1422Ala
ENST00000414678.6:c.2830C>G	ENSP00000412835.2:p.Pro944Ala
NM_017519.2:c.4264C>G	NP_059989.2:p.Pro1422Ala
NM_020732.3:c.4303C>G	NP_065783.3:p.Pro1435Ala
XM_005267069.3:c.4423C>G	XP_005267126.2:p.Pro1475Ala
XM_011535984.1:c.3502C>G	XP_011534286.1:p.Pro1168Ala
XM_011535985.1:c.3322C>G	XP_011534287.1:p.Pro1108Ala
XM_011535986.1:c.3082C>G	XP_011534288.1:p.Pro1028Ala
XM_011535987.1:c.2701C>G	XP_011534289.1:p.Pro901Ala
XM_011535988.1:c.1564C>G	XP_011534290.1:p.Pro522Ala
NM_001346813.1:c.4423C>G	NP_001333742.1:p.Pro1475Ala
NM_001363725.1:c.2173C>G	NP_001350654.1:p.Pro725Ala
XM_011535984.2:c.4633C>G	XP_011534286.2:p.Pro1545Ala
XM_011535988.3:c.1564C>G	XP_011534290.1:p.Pro522Ala
XM_017011103.2:c.4534C>G	XP_016866592.1:p.Pro1512Ala
XM_017011104.1:c.4504C>G	XP_016866593.1:p.Pro1502Ala
XM_017011105.2:c.4474C>G	XP_016866594.1:p.Pro1492Ala
XM_017011106.2:c.4345C>G	XP_016866595.1:p.Pro1449Ala
XM_017011107.2:c.4324C>G	XP_016866596.1:p.Pro1442Ala
XR_002956289.1:n.4619C>G
NM_001363725.2:c.2173C>G	NP_001350654.1:p.Pro725Ala
NM_001371656.1:c.4552C>G	NP_001358585.1:p.Pro1518Ala
NM_001374820.1:c.4552C>G	NP_001361749.1:p.Pro1518Ala
NM_001374828.1:c.4672C>G MANE Select	NP_001361757.1:p.Pro1558Ala
NM_017519.3:c.4513C>G	NP_059989.3:p.Pro1505Ala