Canonical Allele Identifier: CA366242845

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201383-C-A
• MyVariant Identifiers: chr6:g.157522517C>A (hg19) ; chr6:g.157201383C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201383C>A , CM000668.2:g.157201383C>A	GRCh38
NC_000006.11:g.157522517C>A , CM000668.1:g.157522517C>A	GRCh37
NC_000006.10:g.157564209C>A	NCBI36
NG_032093.1:g.428454C>A
NG_032093.2:g.428454C>A
NG_066624.1:g.430358C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4999C>A	ENSP00000055163.8:p.Pro1667Thr
ENST00000414678.8:c.5068C>A	ENSP00000412835.3:p.Pro1690Thr
ENST00000637015.2:c.5287C>A	ENSP00000489729.2:p.Pro1763Thr
ENST00000346085.10:c.5038C>A	ENSP00000344546.5:p.Pro1680Thr
ENST00000350026.10:c.4750C>A	ENSP00000055163.7:p.Pro1584Thr
ENST00000414678.7:c.3316C>A	ENSP00000412835.2:p.Pro1106Thr
ENST00000635849.1:c.2479C>A	ENSP00000490948.1:p.Pro827Thr
ENST00000635957.1:c.2110C>A	ENSP00000490385.1:p.Pro704Thr
ENST00000636227.1:n.3621C>A
ENST00000636254.1:n.1078C>A
ENST00000636930.2:c.5158C>A MANE Select	ENSP00000490491.2:p.Pro1720Thr
ENST00000636940.1:n.3155C>A
ENST00000637015.1:c.2526C>A
ENST00000637568.1:c.2440C>A
ENST00000637741.1:n.1824C>A
ENST00000637810.1:c.2500C>A	ENSP00000489636.1:p.Pro834Thr
ENST00000637904.1:c.2659C>A	ENSP00000490550.1:p.Pro887Thr
ENST00000647938.1:c.4789C>A	ENSP00000498155.1:p.Pro1597Thr
ENST00000346085.9:c.4789C>A	ENSP00000344546.4:p.Pro1597Thr
ENST00000350026.9:c.4750C>A	ENSP00000055163.7:p.Pro1584Thr
ENST00000414678.6:c.3316C>A	ENSP00000412835.2:p.Pro1106Thr
NM_017519.2:c.4750C>A	NP_059989.2:p.Pro1584Thr
NM_020732.3:c.4789C>A	NP_065783.3:p.Pro1597Thr
XM_005267069.3:c.4909C>A	XP_005267126.2:p.Pro1637Thr
XM_011535984.1:c.3988C>A	XP_011534286.1:p.Pro1330Thr
XM_011535985.1:c.3808C>A	XP_011534287.1:p.Pro1270Thr
XM_011535986.1:c.3568C>A	XP_011534288.1:p.Pro1190Thr
XM_011535987.1:c.3187C>A	XP_011534289.1:p.Pro1063Thr
XM_011535988.1:c.2050C>A	XP_011534290.1:p.Pro684Thr
NM_001346813.1:c.4909C>A	NP_001333742.1:p.Pro1637Thr
NM_001363725.1:c.2659C>A	NP_001350654.1:p.Pro887Thr
XM_011535984.2:c.5119C>A	XP_011534286.2:p.Pro1707Thr
XM_011535988.3:c.2050C>A	XP_011534290.1:p.Pro684Thr
XM_017011103.2:c.5020C>A	XP_016866592.1:p.Pro1674Thr
XM_017011104.1:c.4990C>A	XP_016866593.1:p.Pro1664Thr
XM_017011105.2:c.4960C>A	XP_016866594.1:p.Pro1654Thr
XM_017011106.2:c.4831C>A	XP_016866595.1:p.Pro1611Thr
XM_017011107.2:c.4810C>A	XP_016866596.1:p.Pro1604Thr
XR_002956289.1:n.5105C>A
NM_001363725.2:c.2659C>A	NP_001350654.1:p.Pro887Thr
NM_001371656.1:c.5038C>A	NP_001358585.1:p.Pro1680Thr
NM_001374820.1:c.5038C>A	NP_001361749.1:p.Pro1680Thr
NM_001374828.1:c.5158C>A MANE Select	NP_001361757.1:p.Pro1720Thr
NM_017519.3:c.4999C>A	NP_059989.3:p.Pro1667Thr