Canonical Allele Identifier: CA4067719

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1290514
• ClinVar RCV Id: RCV001716628 ; RCV001821961
• dbSNP Id: rs765827636
• ExAC: 6:157522190 C / T
• gnomAD v2: 6-157522190-C-T
• gnomAD v3: 6-157201056-C-T
• gnomAD v4: 6-157201056-C-T
• MyVariant Identifiers: chr6:g.157522190C>T (hg19) ; chr6:g.157201056C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201056C>T , CM000668.2:g.157201056C>T	GRCh38
NC_000006.11:g.157522190C>T , CM000668.1:g.157522190C>T	GRCh37
NC_000006.10:g.157563882C>T	NCBI36
NG_032093.1:g.428127C>T
NG_032093.2:g.428127C>T
NG_066624.1:g.430031C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4672C>T	ENSP00000055163.8:p.Pro1558Ser
ENST00000414678.8:c.4741C>T	ENSP00000412835.3:p.Pro1581Ser
ENST00000637015.2:c.4960C>T	ENSP00000489729.2:p.Pro1654Ser
ENST00000346085.10:c.4711C>T	ENSP00000344546.5:p.Pro1571Ser
ENST00000350026.10:c.4423C>T	ENSP00000055163.7:p.Pro1475Ser
ENST00000414678.7:c.2989C>T	ENSP00000412835.2:p.Pro997Ser
ENST00000635849.1:c.2152C>T	ENSP00000490948.1:p.Pro718Ser
ENST00000635957.1:c.1783C>T	ENSP00000490385.1:p.Pro595Ser
ENST00000636227.1:n.3294C>T
ENST00000636254.1:n.751C>T
ENST00000636930.2:c.4831C>T MANE Select	ENSP00000490491.2:p.Pro1611Ser
ENST00000636940.1:n.2828C>T
ENST00000637015.1:c.2199C>T
ENST00000637568.1:c.2113C>T
ENST00000637741.1:n.1497C>T
ENST00000637810.1:c.2173C>T	ENSP00000489636.1:p.Pro725Ser
ENST00000637904.1:c.2332C>T	ENSP00000490550.1:p.Pro778Ser
ENST00000647938.1:c.4462C>T	ENSP00000498155.1:p.Pro1488Ser
ENST00000346085.9:c.4462C>T	ENSP00000344546.4:p.Pro1488Ser
ENST00000350026.9:c.4423C>T	ENSP00000055163.7:p.Pro1475Ser
ENST00000414678.6:c.2989C>T	ENSP00000412835.2:p.Pro997Ser
NM_017519.2:c.4423C>T	NP_059989.2:p.Pro1475Ser
NM_020732.3:c.4462C>T	NP_065783.3:p.Pro1488Ser
XM_005267069.3:c.4582C>T	XP_005267126.2:p.Pro1528Ser
XM_011535984.1:c.3661C>T	XP_011534286.1:p.Pro1221Ser
XM_011535985.1:c.3481C>T	XP_011534287.1:p.Pro1161Ser
XM_011535986.1:c.3241C>T	XP_011534288.1:p.Pro1081Ser
XM_011535987.1:c.2860C>T	XP_011534289.1:p.Pro954Ser
XM_011535988.1:c.1723C>T	XP_011534290.1:p.Pro575Ser
NM_001346813.1:c.4582C>T	NP_001333742.1:p.Pro1528Ser
NM_001363725.1:c.2332C>T	NP_001350654.1:p.Pro778Ser
XM_011535984.2:c.4792C>T	XP_011534286.2:p.Pro1598Ser
XM_011535988.3:c.1723C>T	XP_011534290.1:p.Pro575Ser
XM_017011103.2:c.4693C>T	XP_016866592.1:p.Pro1565Ser
XM_017011104.1:c.4663C>T	XP_016866593.1:p.Pro1555Ser
XM_017011105.2:c.4633C>T	XP_016866594.1:p.Pro1545Ser
XM_017011106.2:c.4504C>T	XP_016866595.1:p.Pro1502Ser
XM_017011107.2:c.4483C>T	XP_016866596.1:p.Pro1495Ser
XR_002956289.1:n.4778C>T
NM_001363725.2:c.2332C>T	NP_001350654.1:p.Pro778Ser
NM_001371656.1:c.4711C>T	NP_001358585.1:p.Pro1571Ser
NM_001374820.1:c.4711C>T	NP_001361749.1:p.Pro1571Ser
NM_001374828.1:c.4831C>T MANE Select	NP_001361757.1:p.Pro1611Ser
NM_017519.3:c.4672C>T	NP_059989.3:p.Pro1558Ser