Canonical Allele Identifier: CA366234210

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510880C>G (hg19) ; chr6:g.157189746C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189746C>G , CM000668.2:g.157189746C>G	GRCh38
NC_000006.11:g.157510880C>G , CM000668.1:g.157510880C>G	GRCh37
NC_000006.10:g.157552572C>G	NCBI36
NG_032093.1:g.416817C>G
NG_032093.2:g.416817C>G
NG_066624.1:g.418721C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3865C>G	ENSP00000055163.8:p.Pro1289Ala
ENST00000414678.8:c.3934C>G	ENSP00000412835.3:p.Pro1312Ala
ENST00000637015.2:c.4153C>G	ENSP00000489729.2:p.Pro1385Ala
ENST00000346085.10:c.3904C>G	ENSP00000344546.5:p.Pro1302Ala
ENST00000350026.10:c.3616C>G	ENSP00000055163.7:p.Pro1206Ala
ENST00000414678.7:c.2182C>G	ENSP00000412835.2:p.Pro728Ala
ENST00000635849.1:c.1345C>G	ENSP00000490948.1:p.Pro449Ala
ENST00000635957.1:c.979C>G	ENSP00000490385.1:p.Pro327Ala
ENST00000636930.2:c.4024C>G MANE Select	ENSP00000490491.2:p.Pro1342Ala
ENST00000636940.1:n.2021C>G
ENST00000637015.1:c.1392C>G
ENST00000637568.1:c.1306C>G
ENST00000637741.1:n.690C>G
ENST00000637810.1:c.1366C>G	ENSP00000489636.1:p.Pro456Ala
ENST00000637904.1:c.1525C>G	ENSP00000490550.1:p.Pro509Ala
ENST00000647938.1:c.3655C>G	ENSP00000498155.1:p.Pro1219Ala
ENST00000346085.9:c.3655C>G	ENSP00000344546.4:p.Pro1219Ala
ENST00000350026.9:c.3616C>G	ENSP00000055163.7:p.Pro1206Ala
ENST00000414678.6:c.2182C>G	ENSP00000412835.2:p.Pro728Ala
NM_017519.2:c.3616C>G	NP_059989.2:p.Pro1206Ala
NM_020732.3:c.3655C>G	NP_065783.3:p.Pro1219Ala
XM_005267069.3:c.3775C>G	XP_005267126.2:p.Pro1259Ala
XM_011535984.1:c.2854C>G	XP_011534286.1:p.Pro952Ala
XM_011535985.1:c.2674C>G	XP_011534287.1:p.Pro892Ala
XM_011535986.1:c.2434C>G	XP_011534288.1:p.Pro812Ala
XM_011535987.1:c.2053C>G	XP_011534289.1:p.Pro685Ala
XM_011535988.1:c.916C>G	XP_011534290.1:p.Pro306Ala
NM_001346813.1:c.3775C>G	NP_001333742.1:p.Pro1259Ala
NM_001363725.1:c.1525C>G	NP_001350654.1:p.Pro509Ala
XM_011535984.2:c.3985C>G	XP_011534286.2:p.Pro1329Ala
XM_011535988.3:c.916C>G	XP_011534290.1:p.Pro306Ala
XM_017011103.2:c.3886C>G	XP_016866592.1:p.Pro1296Ala
XM_017011104.1:c.3856C>G	XP_016866593.1:p.Pro1286Ala
XM_017011105.2:c.3826C>G	XP_016866594.1:p.Pro1276Ala
XM_017011106.2:c.3697C>G	XP_016866595.1:p.Pro1233Ala
XM_017011107.2:c.3676C>G	XP_016866596.1:p.Pro1226Ala
XR_002956289.1:n.4068C>G
NM_001363725.2:c.1525C>G	NP_001350654.1:p.Pro509Ala
NM_001371656.1:c.3904C>G	NP_001358585.1:p.Pro1302Ala
NM_001374820.1:c.3904C>G	NP_001361749.1:p.Pro1302Ala
NM_001374828.1:c.4024C>G MANE Select	NP_001361757.1:p.Pro1342Ala
NM_017519.3:c.3865C>G	NP_059989.3:p.Pro1289Ala