Canonical Allele Identifier: CA366234873

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190063-C-T
• MyVariant Identifiers: chr6:g.157511197C>T (hg19) ; chr6:g.157190063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190063C>T , CM000668.2:g.157190063C>T	GRCh38
NC_000006.11:g.157511197C>T , CM000668.1:g.157511197C>T	GRCh37
NC_000006.10:g.157552889C>T	NCBI36
NG_032093.1:g.417134C>T
NG_032093.2:g.417134C>T
NG_066624.1:g.419038C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3925C>T	ENSP00000055163.8:p.Pro1309Ser
ENST00000414678.8:c.3994C>T	ENSP00000412835.3:p.Pro1332Ser
ENST00000637015.2:c.4213C>T	ENSP00000489729.2:p.Pro1405Ser
ENST00000346085.10:c.3964C>T	ENSP00000344546.5:p.Pro1322Ser
ENST00000350026.10:c.3676C>T	ENSP00000055163.7:p.Pro1226Ser
ENST00000414678.7:c.2242C>T	ENSP00000412835.2:p.Pro748Ser
ENST00000635849.1:c.1405C>T	ENSP00000490948.1:p.Pro469Ser
ENST00000635957.1:c.1036C>T	ENSP00000490385.1:p.Pro346Ser
ENST00000636930.2:c.4084C>T MANE Select	ENSP00000490491.2:p.Pro1362Ser
ENST00000636940.1:n.2081C>T
ENST00000637015.1:c.1452C>T
ENST00000637568.1:c.1366C>T
ENST00000637741.1:n.750C>T
ENST00000637810.1:c.1426C>T	ENSP00000489636.1:p.Pro476Ser
ENST00000637904.1:c.1585C>T	ENSP00000490550.1:p.Pro529Ser
ENST00000647938.1:c.3715C>T	ENSP00000498155.1:p.Pro1239Ser
ENST00000346085.9:c.3715C>T	ENSP00000344546.4:p.Pro1239Ser
ENST00000350026.9:c.3676C>T	ENSP00000055163.7:p.Pro1226Ser
ENST00000414678.6:c.2242C>T	ENSP00000412835.2:p.Pro748Ser
NM_017519.2:c.3676C>T	NP_059989.2:p.Pro1226Ser
NM_020732.3:c.3715C>T	NP_065783.3:p.Pro1239Ser
XM_005267069.3:c.3835C>T	XP_005267126.2:p.Pro1279Ser
XM_011535984.1:c.2914C>T	XP_011534286.1:p.Pro972Ser
XM_011535985.1:c.2734C>T	XP_011534287.1:p.Pro912Ser
XM_011535986.1:c.2494C>T	XP_011534288.1:p.Pro832Ser
XM_011535987.1:c.2113C>T	XP_011534289.1:p.Pro705Ser
XM_011535988.1:c.976C>T	XP_011534290.1:p.Pro326Ser
NM_001346813.1:c.3835C>T	NP_001333742.1:p.Pro1279Ser
NM_001363725.1:c.1585C>T	NP_001350654.1:p.Pro529Ser
XM_011535984.2:c.4045C>T	XP_011534286.2:p.Pro1349Ser
XM_011535988.3:c.976C>T	XP_011534290.1:p.Pro326Ser
XM_017011103.2:c.3946C>T	XP_016866592.1:p.Pro1316Ser
XM_017011104.1:c.3916C>T	XP_016866593.1:p.Pro1306Ser
XM_017011105.2:c.3886C>T	XP_016866594.1:p.Pro1296Ser
XM_017011106.2:c.3757C>T	XP_016866595.1:p.Pro1253Ser
XM_017011107.2:c.3736C>T	XP_016866596.1:p.Pro1246Ser
XR_002956289.1:n.4128C>T
NM_001363725.2:c.1585C>T	NP_001350654.1:p.Pro529Ser
NM_001371656.1:c.3964C>T	NP_001358585.1:p.Pro1322Ser
NM_001374820.1:c.3964C>T	NP_001361749.1:p.Pro1322Ser
NM_001374828.1:c.4084C>T MANE Select	NP_001361757.1:p.Pro1362Ser
NM_017519.3:c.3925C>T	NP_059989.3:p.Pro1309Ser