Canonical Allele Identifier: CA366242892

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5008C>G	ENSP00000055163.8:p.Pro1670Ala
ENST00000414678.8:c.5077C>G	ENSP00000412835.3:p.Pro1693Ala
ENST00000637015.2:c.5296C>G	ENSP00000489729.2:p.Pro1766Ala
ENST00000346085.10:c.5047C>G	ENSP00000344546.5:p.Pro1683Ala
ENST00000350026.10:c.4759C>G	ENSP00000055163.7:p.Pro1587Ala
ENST00000414678.7:c.3325C>G	ENSP00000412835.2:p.Pro1109Ala
ENST00000635849.1:c.2488C>G	ENSP00000490948.1:p.Pro830Ala
ENST00000635957.1:c.2119C>G	ENSP00000490385.1:p.Pro707Ala
ENST00000636227.1:n.3630C>G
ENST00000636254.1:n.1087C>G
ENST00000636930.2:c.5167C>G MANE Select	ENSP00000490491.2:p.Pro1723Ala
ENST00000636940.1:n.3164C>G
ENST00000637015.1:c.2535C>G
ENST00000637568.1:c.2449C>G
ENST00000637741.1:n.1833C>G
ENST00000637810.1:c.2509C>G	ENSP00000489636.1:p.Pro837Ala
ENST00000637904.1:c.2668C>G	ENSP00000490550.1:p.Pro890Ala
ENST00000647938.1:c.4798C>G	ENSP00000498155.1:p.Pro1600Ala
ENST00000346085.9:c.4798C>G	ENSP00000344546.4:p.Pro1600Ala
ENST00000350026.9:c.4759C>G	ENSP00000055163.7:p.Pro1587Ala
ENST00000414678.6:c.3325C>G	ENSP00000412835.2:p.Pro1109Ala
NM_017519.2:c.4759C>G	NP_059989.2:p.Pro1587Ala
NM_020732.3:c.4798C>G	NP_065783.3:p.Pro1600Ala
XM_005267069.3:c.4918C>G	XP_005267126.2:p.Pro1640Ala
XM_011535984.1:c.3997C>G	XP_011534286.1:p.Pro1333Ala
XM_011535985.1:c.3817C>G	XP_011534287.1:p.Pro1273Ala
XM_011535986.1:c.3577C>G	XP_011534288.1:p.Pro1193Ala
XM_011535987.1:c.3196C>G	XP_011534289.1:p.Pro1066Ala
XM_011535988.1:c.2059C>G	XP_011534290.1:p.Pro687Ala
NM_001346813.1:c.4918C>G	NP_001333742.1:p.Pro1640Ala
NM_001363725.1:c.2668C>G	NP_001350654.1:p.Pro890Ala
XM_011535984.2:c.5128C>G	XP_011534286.2:p.Pro1710Ala
XM_011535988.3:c.2059C>G	XP_011534290.1:p.Pro687Ala
XM_017011103.2:c.5029C>G	XP_016866592.1:p.Pro1677Ala
XM_017011104.1:c.4999C>G	XP_016866593.1:p.Pro1667Ala
XM_017011105.2:c.4969C>G	XP_016866594.1:p.Pro1657Ala
XM_017011106.2:c.4840C>G	XP_016866595.1:p.Pro1614Ala
XM_017011107.2:c.4819C>G	XP_016866596.1:p.Pro1607Ala
XR_002956289.1:n.5114C>G
NM_001363725.2:c.2668C>G	NP_001350654.1:p.Pro890Ala
NM_001371656.1:c.5047C>G	NP_001358585.1:p.Pro1683Ala
NM_001374820.1:c.5047C>G	NP_001361749.1:p.Pro1683Ala
NM_001374828.1:c.5167C>G MANE Select	NP_001361757.1:p.Pro1723Ala
NM_017519.3:c.5008C>G	NP_059989.3:p.Pro1670Ala