Canonical Allele Identifier: CA366234059

Gene: ARID1B

Linked Data

• dbSNP Id: rs752639283
• gnomAD v4: 6-157189674-C-A
• MyVariant Identifiers: chr6:g.157510808C>A (hg19) ; chr6:g.157189674C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189674C>A , CM000668.2:g.157189674C>A	GRCh38
NC_000006.11:g.157510808C>A , CM000668.1:g.157510808C>A	GRCh37
NC_000006.10:g.157552500C>A	NCBI36
NG_032093.1:g.416745C>A
NG_032093.2:g.416745C>A
NG_066624.1:g.418649C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3793C>A	ENSP00000055163.8:p.Pro1265Thr
ENST00000414678.8:c.3862C>A	ENSP00000412835.3:p.Pro1288Thr
ENST00000637015.2:c.4081C>A	ENSP00000489729.2:p.Pro1361Thr
ENST00000346085.10:c.3832C>A	ENSP00000344546.5:p.Pro1278Thr
ENST00000350026.10:c.3544C>A	ENSP00000055163.7:p.Pro1182Thr
ENST00000414678.7:c.2110C>A	ENSP00000412835.2:p.Pro704Thr
ENST00000635849.1:c.1273C>A	ENSP00000490948.1:p.Pro425Thr
ENST00000635957.1:c.907C>A	ENSP00000490385.1:p.Pro303Thr
ENST00000636930.2:c.3952C>A MANE Select	ENSP00000490491.2:p.Pro1318Thr
ENST00000636940.1:n.1949C>A
ENST00000637015.1:c.1320C>A
ENST00000637568.1:c.1234C>A
ENST00000637741.1:n.618C>A
ENST00000637810.1:c.1294C>A	ENSP00000489636.1:p.Pro432Thr
ENST00000637904.1:c.1453C>A	ENSP00000490550.1:p.Pro485Thr
ENST00000647938.1:c.3583C>A	ENSP00000498155.1:p.Pro1195Thr
ENST00000346085.9:c.3583C>A	ENSP00000344546.4:p.Pro1195Thr
ENST00000350026.9:c.3544C>A	ENSP00000055163.7:p.Pro1182Thr
ENST00000414678.6:c.2110C>A	ENSP00000412835.2:p.Pro704Thr
NM_017519.2:c.3544C>A	NP_059989.2:p.Pro1182Thr
NM_020732.3:c.3583C>A	NP_065783.3:p.Pro1195Thr
XM_005267069.3:c.3703C>A	XP_005267126.2:p.Pro1235Thr
XM_011535984.1:c.2782C>A	XP_011534286.1:p.Pro928Thr
XM_011535985.1:c.2602C>A	XP_011534287.1:p.Pro868Thr
XM_011535986.1:c.2362C>A	XP_011534288.1:p.Pro788Thr
XM_011535987.1:c.1981C>A	XP_011534289.1:p.Pro661Thr
XM_011535988.1:c.844C>A	XP_011534290.1:p.Pro282Thr
NM_001346813.1:c.3703C>A	NP_001333742.1:p.Pro1235Thr
NM_001363725.1:c.1453C>A	NP_001350654.1:p.Pro485Thr
XM_011535984.2:c.3913C>A	XP_011534286.2:p.Pro1305Thr
XM_011535988.3:c.844C>A	XP_011534290.1:p.Pro282Thr
XM_017011103.2:c.3814C>A	XP_016866592.1:p.Pro1272Thr
XM_017011104.1:c.3784C>A	XP_016866593.1:p.Pro1262Thr
XM_017011105.2:c.3754C>A	XP_016866594.1:p.Pro1252Thr
XM_017011106.2:c.3625C>A	XP_016866595.1:p.Pro1209Thr
XM_017011107.2:c.3604C>A	XP_016866596.1:p.Pro1202Thr
XR_002956289.1:n.3996C>A
NM_001363725.2:c.1453C>A	NP_001350654.1:p.Pro485Thr
NM_001371656.1:c.3832C>A	NP_001358585.1:p.Pro1278Thr
NM_001374820.1:c.3832C>A	NP_001361749.1:p.Pro1278Thr
NM_001374828.1:c.3952C>A MANE Select	NP_001361757.1:p.Pro1318Thr
NM_017519.3:c.3793C>A	NP_059989.3:p.Pro1265Thr