Canonical Allele Identifier: CA366235181

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339686
• gnomAD v4: 6-157190093-C-T
• MyVariant Identifiers: chr6:g.157511227C>T (hg19) ; chr6:g.157190093C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190093C>T , CM000668.2:g.157190093C>T	GRCh38
NC_000006.11:g.157511227C>T , CM000668.1:g.157511227C>T	GRCh37
NC_000006.10:g.157552919C>T	NCBI36
NG_032093.1:g.417164C>T
NG_032093.2:g.417164C>T
NG_066624.1:g.419068C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3955C>T	ENSP00000055163.8:p.Pro1319Ser
ENST00000414678.8:c.4024C>T	ENSP00000412835.3:p.Pro1342Ser
ENST00000637015.2:c.4243C>T	ENSP00000489729.2:p.Pro1415Ser
ENST00000346085.10:c.3994C>T	ENSP00000344546.5:p.Pro1332Ser
ENST00000350026.10:c.3706C>T	ENSP00000055163.7:p.Pro1236Ser
ENST00000414678.7:c.2272C>T	ENSP00000412835.2:p.Pro758Ser
ENST00000635849.1:c.1435C>T	ENSP00000490948.1:p.Pro479Ser
ENST00000635957.1:c.1066C>T	ENSP00000490385.1:p.Pro356Ser
ENST00000636930.2:c.4114C>T MANE Select	ENSP00000490491.2:p.Pro1372Ser
ENST00000636940.1:n.2111C>T
ENST00000637015.1:c.1482C>T
ENST00000637568.1:c.1396C>T
ENST00000637741.1:n.780C>T
ENST00000637810.1:c.1456C>T	ENSP00000489636.1:p.Pro486Ser
ENST00000637904.1:c.1615C>T	ENSP00000490550.1:p.Pro539Ser
ENST00000647938.1:c.3745C>T	ENSP00000498155.1:p.Pro1249Ser
ENST00000346085.9:c.3745C>T	ENSP00000344546.4:p.Pro1249Ser
ENST00000350026.9:c.3706C>T	ENSP00000055163.7:p.Pro1236Ser
ENST00000414678.6:c.2272C>T	ENSP00000412835.2:p.Pro758Ser
NM_017519.2:c.3706C>T	NP_059989.2:p.Pro1236Ser
NM_020732.3:c.3745C>T	NP_065783.3:p.Pro1249Ser
XM_005267069.3:c.3865C>T	XP_005267126.2:p.Pro1289Ser
XM_011535984.1:c.2944C>T	XP_011534286.1:p.Pro982Ser
XM_011535985.1:c.2764C>T	XP_011534287.1:p.Pro922Ser
XM_011535986.1:c.2524C>T	XP_011534288.1:p.Pro842Ser
XM_011535987.1:c.2143C>T	XP_011534289.1:p.Pro715Ser
XM_011535988.1:c.1006C>T	XP_011534290.1:p.Pro336Ser
NM_001346813.1:c.3865C>T	NP_001333742.1:p.Pro1289Ser
NM_001363725.1:c.1615C>T	NP_001350654.1:p.Pro539Ser
XM_011535984.2:c.4075C>T	XP_011534286.2:p.Pro1359Ser
XM_011535988.3:c.1006C>T	XP_011534290.1:p.Pro336Ser
XM_017011103.2:c.3976C>T	XP_016866592.1:p.Pro1326Ser
XM_017011104.1:c.3946C>T	XP_016866593.1:p.Pro1316Ser
XM_017011105.2:c.3916C>T	XP_016866594.1:p.Pro1306Ser
XM_017011106.2:c.3787C>T	XP_016866595.1:p.Pro1263Ser
XM_017011107.2:c.3766C>T	XP_016866596.1:p.Pro1256Ser
XR_002956289.1:n.4158C>T
NM_001363725.2:c.1615C>T	NP_001350654.1:p.Pro539Ser
NM_001371656.1:c.3994C>T	NP_001358585.1:p.Pro1332Ser
NM_001374820.1:c.3994C>T	NP_001361749.1:p.Pro1332Ser
NM_001374828.1:c.4114C>T MANE Select	NP_001361757.1:p.Pro1372Ser
NM_017519.3:c.3955C>T	NP_059989.3:p.Pro1319Ser