Canonical Allele Identifier: CA366242395

Gene: ARID1B

Linked Data

• dbSNP Id: rs1277541274
• gnomAD v2: 6-157522413-C-T
• gnomAD v4: 6-157201279-C-T
• COSMIC: COSM3622286 ; COSM3622287
• MyVariant Identifiers: chr6:g.157522413C>T (hg19) ; chr6:g.157201279C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201279C>T , CM000668.2:g.157201279C>T	GRCh38
NC_000006.11:g.157522413C>T , CM000668.1:g.157522413C>T	GRCh37
NC_000006.10:g.157564105C>T	NCBI36
NG_032093.1:g.428350C>T
NG_032093.2:g.428350C>T
NG_066624.1:g.430254C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4895C>T	ENSP00000055163.8:p.Ser1632Phe
ENST00000414678.8:c.4964C>T	ENSP00000412835.3:p.Ser1655Phe
ENST00000637015.2:c.5183C>T	ENSP00000489729.2:p.Ser1728Phe
ENST00000346085.10:c.4934C>T	ENSP00000344546.5:p.Ser1645Phe
ENST00000350026.10:c.4646C>T	ENSP00000055163.7:p.Ser1549Phe
ENST00000414678.7:c.3212C>T	ENSP00000412835.2:p.Ser1071Phe
ENST00000635849.1:c.2375C>T	ENSP00000490948.1:p.Ser792Phe
ENST00000635957.1:c.2006C>T	ENSP00000490385.1:p.Ser669Phe
ENST00000636227.1:n.3517C>T
ENST00000636254.1:n.974C>T
ENST00000636930.2:c.5054C>T MANE Select	ENSP00000490491.2:p.Ser1685Phe
ENST00000636940.1:n.3051C>T
ENST00000637015.1:c.2422C>T
ENST00000637568.1:c.2336C>T
ENST00000637741.1:n.1720C>T
ENST00000637810.1:c.2396C>T	ENSP00000489636.1:p.Ser799Phe
ENST00000637904.1:c.2555C>T	ENSP00000490550.1:p.Ser852Phe
ENST00000647938.1:c.4685C>T	ENSP00000498155.1:p.Ser1562Phe
ENST00000346085.9:c.4685C>T	ENSP00000344546.4:p.Ser1562Phe
ENST00000350026.9:c.4646C>T	ENSP00000055163.7:p.Ser1549Phe
ENST00000414678.6:c.3212C>T	ENSP00000412835.2:p.Ser1071Phe
NM_017519.2:c.4646C>T	NP_059989.2:p.Ser1549Phe
NM_020732.3:c.4685C>T	NP_065783.3:p.Ser1562Phe
XM_005267069.3:c.4805C>T	XP_005267126.2:p.Ser1602Phe
XM_011535984.1:c.3884C>T	XP_011534286.1:p.Ser1295Phe
XM_011535985.1:c.3704C>T	XP_011534287.1:p.Ser1235Phe
XM_011535986.1:c.3464C>T	XP_011534288.1:p.Ser1155Phe
XM_011535987.1:c.3083C>T	XP_011534289.1:p.Ser1028Phe
XM_011535988.1:c.1946C>T	XP_011534290.1:p.Ser649Phe
NM_001346813.1:c.4805C>T	NP_001333742.1:p.Ser1602Phe
NM_001363725.1:c.2555C>T	NP_001350654.1:p.Ser852Phe
XM_011535984.2:c.5015C>T	XP_011534286.2:p.Ser1672Phe
XM_011535988.3:c.1946C>T	XP_011534290.1:p.Ser649Phe
XM_017011103.2:c.4916C>T	XP_016866592.1:p.Ser1639Phe
XM_017011104.1:c.4886C>T	XP_016866593.1:p.Ser1629Phe
XM_017011105.2:c.4856C>T	XP_016866594.1:p.Ser1619Phe
XM_017011106.2:c.4727C>T	XP_016866595.1:p.Ser1576Phe
XM_017011107.2:c.4706C>T	XP_016866596.1:p.Ser1569Phe
XR_002956289.1:n.5001C>T
NM_001363725.2:c.2555C>T	NP_001350654.1:p.Ser852Phe
NM_001371656.1:c.4934C>T	NP_001358585.1:p.Ser1645Phe
NM_001374820.1:c.4934C>T	NP_001361749.1:p.Ser1645Phe
NM_001374828.1:c.5054C>T MANE Select	NP_001361757.1:p.Ser1685Phe
NM_017519.3:c.4895C>T	NP_059989.3:p.Ser1632Phe