Canonical Allele Identifier: CA366242716

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522490C>G (hg19) ; chr6:g.157201356C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201356C>G , CM000668.2:g.157201356C>G	GRCh38
NC_000006.11:g.157522490C>G , CM000668.1:g.157522490C>G	GRCh37
NC_000006.10:g.157564182C>G	NCBI36
NG_032093.1:g.428427C>G
NG_032093.2:g.428427C>G
NG_066624.1:g.430331C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4972C>G	ENSP00000055163.8:p.Pro1658Ala
ENST00000414678.8:c.5041C>G	ENSP00000412835.3:p.Pro1681Ala
ENST00000637015.2:c.5260C>G	ENSP00000489729.2:p.Pro1754Ala
ENST00000346085.10:c.5011C>G	ENSP00000344546.5:p.Pro1671Ala
ENST00000350026.10:c.4723C>G	ENSP00000055163.7:p.Pro1575Ala
ENST00000414678.7:c.3289C>G	ENSP00000412835.2:p.Pro1097Ala
ENST00000635849.1:c.2452C>G	ENSP00000490948.1:p.Pro818Ala
ENST00000635957.1:c.2083C>G	ENSP00000490385.1:p.Pro695Ala
ENST00000636227.1:n.3594C>G
ENST00000636254.1:n.1051C>G
ENST00000636930.2:c.5131C>G MANE Select	ENSP00000490491.2:p.Pro1711Ala
ENST00000636940.1:n.3128C>G
ENST00000637015.1:c.2499C>G
ENST00000637568.1:c.2413C>G
ENST00000637741.1:n.1797C>G
ENST00000637810.1:c.2473C>G	ENSP00000489636.1:p.Pro825Ala
ENST00000637904.1:c.2632C>G	ENSP00000490550.1:p.Pro878Ala
ENST00000647938.1:c.4762C>G	ENSP00000498155.1:p.Pro1588Ala
ENST00000346085.9:c.4762C>G	ENSP00000344546.4:p.Pro1588Ala
ENST00000350026.9:c.4723C>G	ENSP00000055163.7:p.Pro1575Ala
ENST00000414678.6:c.3289C>G	ENSP00000412835.2:p.Pro1097Ala
NM_017519.2:c.4723C>G	NP_059989.2:p.Pro1575Ala
NM_020732.3:c.4762C>G	NP_065783.3:p.Pro1588Ala
XM_005267069.3:c.4882C>G	XP_005267126.2:p.Pro1628Ala
XM_011535984.1:c.3961C>G	XP_011534286.1:p.Pro1321Ala
XM_011535985.1:c.3781C>G	XP_011534287.1:p.Pro1261Ala
XM_011535986.1:c.3541C>G	XP_011534288.1:p.Pro1181Ala
XM_011535987.1:c.3160C>G	XP_011534289.1:p.Pro1054Ala
XM_011535988.1:c.2023C>G	XP_011534290.1:p.Pro675Ala
NM_001346813.1:c.4882C>G	NP_001333742.1:p.Pro1628Ala
NM_001363725.1:c.2632C>G	NP_001350654.1:p.Pro878Ala
XM_011535984.2:c.5092C>G	XP_011534286.2:p.Pro1698Ala
XM_011535988.3:c.2023C>G	XP_011534290.1:p.Pro675Ala
XM_017011103.2:c.4993C>G	XP_016866592.1:p.Pro1665Ala
XM_017011104.1:c.4963C>G	XP_016866593.1:p.Pro1655Ala
XM_017011105.2:c.4933C>G	XP_016866594.1:p.Pro1645Ala
XM_017011106.2:c.4804C>G	XP_016866595.1:p.Pro1602Ala
XM_017011107.2:c.4783C>G	XP_016866596.1:p.Pro1595Ala
XR_002956289.1:n.5078C>G
NM_001363725.2:c.2632C>G	NP_001350654.1:p.Pro878Ala
NM_001371656.1:c.5011C>G	NP_001358585.1:p.Pro1671Ala
NM_001374820.1:c.5011C>G	NP_001361749.1:p.Pro1671Ala
NM_001374828.1:c.5131C>G MANE Select	NP_001361757.1:p.Pro1711Ala
NM_017519.3:c.4972C>G	NP_059989.3:p.Pro1658Ala