Canonical Allele Identifier: CA366242513

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522454C>G (hg19) ; chr6:g.157201320C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201320C>G , CM000668.2:g.157201320C>G	GRCh38
NC_000006.11:g.157522454C>G , CM000668.1:g.157522454C>G	GRCh37
NC_000006.10:g.157564146C>G	NCBI36
NG_032093.1:g.428391C>G
NG_032093.2:g.428391C>G
NG_066624.1:g.430295C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4936C>G	ENSP00000055163.8:p.Pro1646Ala
ENST00000414678.8:c.5005C>G	ENSP00000412835.3:p.Pro1669Ala
ENST00000637015.2:c.5224C>G	ENSP00000489729.2:p.Pro1742Ala
ENST00000346085.10:c.4975C>G	ENSP00000344546.5:p.Pro1659Ala
ENST00000350026.10:c.4687C>G	ENSP00000055163.7:p.Pro1563Ala
ENST00000414678.7:c.3253C>G	ENSP00000412835.2:p.Pro1085Ala
ENST00000635849.1:c.2416C>G	ENSP00000490948.1:p.Pro806Ala
ENST00000635957.1:c.2047C>G	ENSP00000490385.1:p.Pro683Ala
ENST00000636227.1:n.3558C>G
ENST00000636254.1:n.1015C>G
ENST00000636930.2:c.5095C>G MANE Select	ENSP00000490491.2:p.Pro1699Ala
ENST00000636940.1:n.3092C>G
ENST00000637015.1:c.2463C>G
ENST00000637568.1:c.2377C>G
ENST00000637741.1:n.1761C>G
ENST00000637810.1:c.2437C>G	ENSP00000489636.1:p.Pro813Ala
ENST00000637904.1:c.2596C>G	ENSP00000490550.1:p.Pro866Ala
ENST00000647938.1:c.4726C>G	ENSP00000498155.1:p.Pro1576Ala
ENST00000346085.9:c.4726C>G	ENSP00000344546.4:p.Pro1576Ala
ENST00000350026.9:c.4687C>G	ENSP00000055163.7:p.Pro1563Ala
ENST00000414678.6:c.3253C>G	ENSP00000412835.2:p.Pro1085Ala
NM_017519.2:c.4687C>G	NP_059989.2:p.Pro1563Ala
NM_020732.3:c.4726C>G	NP_065783.3:p.Pro1576Ala
XM_005267069.3:c.4846C>G	XP_005267126.2:p.Pro1616Ala
XM_011535984.1:c.3925C>G	XP_011534286.1:p.Pro1309Ala
XM_011535985.1:c.3745C>G	XP_011534287.1:p.Pro1249Ala
XM_011535986.1:c.3505C>G	XP_011534288.1:p.Pro1169Ala
XM_011535987.1:c.3124C>G	XP_011534289.1:p.Pro1042Ala
XM_011535988.1:c.1987C>G	XP_011534290.1:p.Pro663Ala
NM_001346813.1:c.4846C>G	NP_001333742.1:p.Pro1616Ala
NM_001363725.1:c.2596C>G	NP_001350654.1:p.Pro866Ala
XM_011535984.2:c.5056C>G	XP_011534286.2:p.Pro1686Ala
XM_011535988.3:c.1987C>G	XP_011534290.1:p.Pro663Ala
XM_017011103.2:c.4957C>G	XP_016866592.1:p.Pro1653Ala
XM_017011104.1:c.4927C>G	XP_016866593.1:p.Pro1643Ala
XM_017011105.2:c.4897C>G	XP_016866594.1:p.Pro1633Ala
XM_017011106.2:c.4768C>G	XP_016866595.1:p.Pro1590Ala
XM_017011107.2:c.4747C>G	XP_016866596.1:p.Pro1583Ala
XR_002956289.1:n.5042C>G
NM_001363725.2:c.2596C>G	NP_001350654.1:p.Pro866Ala
NM_001371656.1:c.4975C>G	NP_001358585.1:p.Pro1659Ala
NM_001374820.1:c.4975C>G	NP_001361749.1:p.Pro1659Ala
NM_001374828.1:c.5095C>G MANE Select	NP_001361757.1:p.Pro1699Ala
NM_017519.3:c.4936C>G	NP_059989.3:p.Pro1646Ala