Canonical Allele Identifier: CA4067769

Gene: ARID1B

Linked Data

• dbSNP Id: rs775920998
• ExAC: 6:157522526 C / T
• gnomAD v2: 6-157522526-C-T
• gnomAD v4: 6-157201392-C-T
• MyVariant Identifiers: chr6:g.157522526C>T (hg19) ; chr6:g.157201392C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201392C>T , CM000668.2:g.157201392C>T	GRCh38
NC_000006.11:g.157522526C>T , CM000668.1:g.157522526C>T	GRCh37
NC_000006.10:g.157564218C>T	NCBI36
NG_032093.1:g.428463C>T
NG_032093.2:g.428463C>T
NG_066624.1:g.430367C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5008C>T	ENSP00000055163.8:p.Pro1670Ser
ENST00000414678.8:c.5077C>T	ENSP00000412835.3:p.Pro1693Ser
ENST00000637015.2:c.5296C>T	ENSP00000489729.2:p.Pro1766Ser
ENST00000346085.10:c.5047C>T	ENSP00000344546.5:p.Pro1683Ser
ENST00000350026.10:c.4759C>T	ENSP00000055163.7:p.Pro1587Ser
ENST00000414678.7:c.3325C>T	ENSP00000412835.2:p.Pro1109Ser
ENST00000635849.1:c.2488C>T	ENSP00000490948.1:p.Pro830Ser
ENST00000635957.1:c.2119C>T	ENSP00000490385.1:p.Pro707Ser
ENST00000636227.1:n.3630C>T
ENST00000636254.1:n.1087C>T
ENST00000636930.2:c.5167C>T MANE Select	ENSP00000490491.2:p.Pro1723Ser
ENST00000636940.1:n.3164C>T
ENST00000637015.1:c.2535C>T
ENST00000637568.1:c.2449C>T
ENST00000637741.1:n.1833C>T
ENST00000637810.1:c.2509C>T	ENSP00000489636.1:p.Pro837Ser
ENST00000637904.1:c.2668C>T	ENSP00000490550.1:p.Pro890Ser
ENST00000647938.1:c.4798C>T	ENSP00000498155.1:p.Pro1600Ser
ENST00000346085.9:c.4798C>T	ENSP00000344546.4:p.Pro1600Ser
ENST00000350026.9:c.4759C>T	ENSP00000055163.7:p.Pro1587Ser
ENST00000414678.6:c.3325C>T	ENSP00000412835.2:p.Pro1109Ser
NM_017519.2:c.4759C>T	NP_059989.2:p.Pro1587Ser
NM_020732.3:c.4798C>T	NP_065783.3:p.Pro1600Ser
XM_005267069.3:c.4918C>T	XP_005267126.2:p.Pro1640Ser
XM_011535984.1:c.3997C>T	XP_011534286.1:p.Pro1333Ser
XM_011535985.1:c.3817C>T	XP_011534287.1:p.Pro1273Ser
XM_011535986.1:c.3577C>T	XP_011534288.1:p.Pro1193Ser
XM_011535987.1:c.3196C>T	XP_011534289.1:p.Pro1066Ser
XM_011535988.1:c.2059C>T	XP_011534290.1:p.Pro687Ser
NM_001346813.1:c.4918C>T	NP_001333742.1:p.Pro1640Ser
NM_001363725.1:c.2668C>T	NP_001350654.1:p.Pro890Ser
XM_011535984.2:c.5128C>T	XP_011534286.2:p.Pro1710Ser
XM_011535988.3:c.2059C>T	XP_011534290.1:p.Pro687Ser
XM_017011103.2:c.5029C>T	XP_016866592.1:p.Pro1677Ser
XM_017011104.1:c.4999C>T	XP_016866593.1:p.Pro1667Ser
XM_017011105.2:c.4969C>T	XP_016866594.1:p.Pro1657Ser
XM_017011106.2:c.4840C>T	XP_016866595.1:p.Pro1614Ser
XM_017011107.2:c.4819C>T	XP_016866596.1:p.Pro1607Ser
XR_002956289.1:n.5114C>T
NM_001363725.2:c.2668C>T	NP_001350654.1:p.Pro890Ser
NM_001371656.1:c.5047C>T	NP_001358585.1:p.Pro1683Ser
NM_001374820.1:c.5047C>T	NP_001361749.1:p.Pro1683Ser
NM_001374828.1:c.5167C>T MANE Select	NP_001361757.1:p.Pro1723Ser
NM_017519.3:c.5008C>T	NP_059989.3:p.Pro1670Ser