Canonical Allele Identifier: CA366242897

Gene: ARID1B

Linked Data

• dbSNP Id: rs1728897975
• gnomAD v3: 6-157201393-C-T
• gnomAD v4: 6-157201393-C-T
• MyVariant Identifiers: chr6:g.157522527C>T (hg19) ; chr6:g.157201393C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201393C>T , CM000668.2:g.157201393C>T	GRCh38
NC_000006.11:g.157522527C>T , CM000668.1:g.157522527C>T	GRCh37
NC_000006.10:g.157564219C>T	NCBI36
NG_032093.1:g.428464C>T
NG_032093.2:g.428464C>T
NG_066624.1:g.430368C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5009C>T	ENSP00000055163.8:p.Pro1670Leu
ENST00000414678.8:c.5078C>T	ENSP00000412835.3:p.Pro1693Leu
ENST00000637015.2:c.5297C>T	ENSP00000489729.2:p.Pro1766Leu
ENST00000346085.10:c.5048C>T	ENSP00000344546.5:p.Pro1683Leu
ENST00000350026.10:c.4760C>T	ENSP00000055163.7:p.Pro1587Leu
ENST00000414678.7:c.3326C>T	ENSP00000412835.2:p.Pro1109Leu
ENST00000635849.1:c.2489C>T	ENSP00000490948.1:p.Pro830Leu
ENST00000635957.1:c.2120C>T	ENSP00000490385.1:p.Pro707Leu
ENST00000636227.1:n.3631C>T
ENST00000636254.1:n.1088C>T
ENST00000636930.2:c.5168C>T MANE Select	ENSP00000490491.2:p.Pro1723Leu
ENST00000636940.1:n.3165C>T
ENST00000637015.1:c.2536C>T
ENST00000637568.1:c.2450C>T
ENST00000637741.1:n.1834C>T
ENST00000637810.1:c.2510C>T	ENSP00000489636.1:p.Pro837Leu
ENST00000637904.1:c.2669C>T	ENSP00000490550.1:p.Pro890Leu
ENST00000647938.1:c.4799C>T	ENSP00000498155.1:p.Pro1600Leu
ENST00000346085.9:c.4799C>T	ENSP00000344546.4:p.Pro1600Leu
ENST00000350026.9:c.4760C>T	ENSP00000055163.7:p.Pro1587Leu
ENST00000414678.6:c.3326C>T	ENSP00000412835.2:p.Pro1109Leu
NM_017519.2:c.4760C>T	NP_059989.2:p.Pro1587Leu
NM_020732.3:c.4799C>T	NP_065783.3:p.Pro1600Leu
XM_005267069.3:c.4919C>T	XP_005267126.2:p.Pro1640Leu
XM_011535984.1:c.3998C>T	XP_011534286.1:p.Pro1333Leu
XM_011535985.1:c.3818C>T	XP_011534287.1:p.Pro1273Leu
XM_011535986.1:c.3578C>T	XP_011534288.1:p.Pro1193Leu
XM_011535987.1:c.3197C>T	XP_011534289.1:p.Pro1066Leu
XM_011535988.1:c.2060C>T	XP_011534290.1:p.Pro687Leu
NM_001346813.1:c.4919C>T	NP_001333742.1:p.Pro1640Leu
NM_001363725.1:c.2669C>T	NP_001350654.1:p.Pro890Leu
XM_011535984.2:c.5129C>T	XP_011534286.2:p.Pro1710Leu
XM_011535988.3:c.2060C>T	XP_011534290.1:p.Pro687Leu
XM_017011103.2:c.5030C>T	XP_016866592.1:p.Pro1677Leu
XM_017011104.1:c.5000C>T	XP_016866593.1:p.Pro1667Leu
XM_017011105.2:c.4970C>T	XP_016866594.1:p.Pro1657Leu
XM_017011106.2:c.4841C>T	XP_016866595.1:p.Pro1614Leu
XM_017011107.2:c.4820C>T	XP_016866596.1:p.Pro1607Leu
XR_002956289.1:n.5115C>T
NM_001363725.2:c.2669C>T	NP_001350654.1:p.Pro890Leu
NM_001371656.1:c.5048C>T	NP_001358585.1:p.Pro1683Leu
NM_001374820.1:c.5048C>T	NP_001361749.1:p.Pro1683Leu
NM_001374828.1:c.5168C>T MANE Select	NP_001361757.1:p.Pro1723Leu
NM_017519.3:c.5009C>T	NP_059989.3:p.Pro1670Leu