Canonical Allele Identifier: CA366234209

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339001
• MyVariant Identifiers: chr6:g.157510880C>A (hg19) ; chr6:g.157189746C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3865C>A	ENSP00000055163.8:p.Pro1289Thr
ENST00000414678.8:c.3934C>A	ENSP00000412835.3:p.Pro1312Thr
ENST00000637015.2:c.4153C>A	ENSP00000489729.2:p.Pro1385Thr
ENST00000346085.10:c.3904C>A	ENSP00000344546.5:p.Pro1302Thr
ENST00000350026.10:c.3616C>A	ENSP00000055163.7:p.Pro1206Thr
ENST00000414678.7:c.2182C>A	ENSP00000412835.2:p.Pro728Thr
ENST00000635849.1:c.1345C>A	ENSP00000490948.1:p.Pro449Thr
ENST00000635957.1:c.979C>A	ENSP00000490385.1:p.Pro327Thr
ENST00000636930.2:c.4024C>A MANE Select	ENSP00000490491.2:p.Pro1342Thr
ENST00000636940.1:n.2021C>A
ENST00000637015.1:c.1392C>A
ENST00000637568.1:c.1306C>A
ENST00000637741.1:n.690C>A
ENST00000637810.1:c.1366C>A	ENSP00000489636.1:p.Pro456Thr
ENST00000637904.1:c.1525C>A	ENSP00000490550.1:p.Pro509Thr
ENST00000647938.1:c.3655C>A	ENSP00000498155.1:p.Pro1219Thr
ENST00000346085.9:c.3655C>A	ENSP00000344546.4:p.Pro1219Thr
ENST00000350026.9:c.3616C>A	ENSP00000055163.7:p.Pro1206Thr
ENST00000414678.6:c.2182C>A	ENSP00000412835.2:p.Pro728Thr
NM_017519.2:c.3616C>A	NP_059989.2:p.Pro1206Thr
NM_020732.3:c.3655C>A	NP_065783.3:p.Pro1219Thr
XM_005267069.3:c.3775C>A	XP_005267126.2:p.Pro1259Thr
XM_011535984.1:c.2854C>A	XP_011534286.1:p.Pro952Thr
XM_011535985.1:c.2674C>A	XP_011534287.1:p.Pro892Thr
XM_011535986.1:c.2434C>A	XP_011534288.1:p.Pro812Thr
XM_011535987.1:c.2053C>A	XP_011534289.1:p.Pro685Thr
XM_011535988.1:c.916C>A	XP_011534290.1:p.Pro306Thr
NM_001346813.1:c.3775C>A	NP_001333742.1:p.Pro1259Thr
NM_001363725.1:c.1525C>A	NP_001350654.1:p.Pro509Thr
XM_011535984.2:c.3985C>A	XP_011534286.2:p.Pro1329Thr
XM_011535988.3:c.916C>A	XP_011534290.1:p.Pro306Thr
XM_017011103.2:c.3886C>A	XP_016866592.1:p.Pro1296Thr
XM_017011104.1:c.3856C>A	XP_016866593.1:p.Pro1286Thr
XM_017011105.2:c.3826C>A	XP_016866594.1:p.Pro1276Thr
XM_017011106.2:c.3697C>A	XP_016866595.1:p.Pro1233Thr
XM_017011107.2:c.3676C>A	XP_016866596.1:p.Pro1226Thr
XR_002956289.1:n.4068C>A
NM_001363725.2:c.1525C>A	NP_001350654.1:p.Pro509Thr
NM_001371656.1:c.3904C>A	NP_001358585.1:p.Pro1302Thr
NM_001374820.1:c.3904C>A	NP_001361749.1:p.Pro1302Thr
NM_001374828.1:c.4024C>A MANE Select	NP_001361757.1:p.Pro1342Thr
NM_017519.3:c.3865C>A	NP_059989.3:p.Pro1289Thr