Canonical Allele Identifier: CA366234003

Gene: ARID1B

Linked Data

• dbSNP Id: rs1402613006
• gnomAD v2: 6-157510781-T-C
• gnomAD v4: 6-157189647-T-C
• MyVariant Identifiers: chr6:g.157510781T>C (hg19) ; chr6:g.157189647T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189647T>C , CM000668.2:g.157189647T>C	GRCh38
NC_000006.11:g.157510781T>C , CM000668.1:g.157510781T>C	GRCh37
NC_000006.10:g.157552473T>C	NCBI36
NG_032093.1:g.416718T>C
NG_032093.2:g.416718T>C
NG_066624.1:g.418622T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3766T>C	ENSP00000055163.8:p.Ser1256Pro
ENST00000414678.8:c.3835T>C	ENSP00000412835.3:p.Ser1279Pro
ENST00000637015.2:c.4054T>C	ENSP00000489729.2:p.Ser1352Pro
ENST00000346085.10:c.3805T>C	ENSP00000344546.5:p.Ser1269Pro
ENST00000350026.10:c.3517T>C	ENSP00000055163.7:p.Ser1173Pro
ENST00000414678.7:c.2083T>C	ENSP00000412835.2:p.Ser695Pro
ENST00000635849.1:c.1246T>C	ENSP00000490948.1:p.Ser416Pro
ENST00000635957.1:c.880T>C	ENSP00000490385.1:p.Ser294Pro
ENST00000636930.2:c.3925T>C MANE Select	ENSP00000490491.2:p.Ser1309Pro
ENST00000636940.1:n.1922T>C
ENST00000637015.1:c.1293T>C
ENST00000637568.1:c.1207T>C
ENST00000637741.1:n.591T>C
ENST00000637810.1:c.1267T>C	ENSP00000489636.1:p.Ser423Pro
ENST00000637904.1:c.1426T>C	ENSP00000490550.1:p.Ser476Pro
ENST00000647938.1:c.3556T>C	ENSP00000498155.1:p.Ser1186Pro
ENST00000346085.9:c.3556T>C	ENSP00000344546.4:p.Ser1186Pro
ENST00000350026.9:c.3517T>C	ENSP00000055163.7:p.Ser1173Pro
ENST00000414678.6:c.2083T>C	ENSP00000412835.2:p.Ser695Pro
NM_017519.2:c.3517T>C	NP_059989.2:p.Ser1173Pro
NM_020732.3:c.3556T>C	NP_065783.3:p.Ser1186Pro
XM_005267069.3:c.3676T>C	XP_005267126.2:p.Ser1226Pro
XM_011535984.1:c.2755T>C	XP_011534286.1:p.Ser919Pro
XM_011535985.1:c.2575T>C	XP_011534287.1:p.Ser859Pro
XM_011535986.1:c.2335T>C	XP_011534288.1:p.Ser779Pro
XM_011535987.1:c.1954T>C	XP_011534289.1:p.Ser652Pro
XM_011535988.1:c.817T>C	XP_011534290.1:p.Ser273Pro
NM_001346813.1:c.3676T>C	NP_001333742.1:p.Ser1226Pro
NM_001363725.1:c.1426T>C	NP_001350654.1:p.Ser476Pro
XM_011535984.2:c.3886T>C	XP_011534286.2:p.Ser1296Pro
XM_011535988.3:c.817T>C	XP_011534290.1:p.Ser273Pro
XM_017011103.2:c.3787T>C	XP_016866592.1:p.Ser1263Pro
XM_017011104.1:c.3757T>C	XP_016866593.1:p.Ser1253Pro
XM_017011105.2:c.3727T>C	XP_016866594.1:p.Ser1243Pro
XM_017011106.2:c.3598T>C	XP_016866595.1:p.Ser1200Pro
XM_017011107.2:c.3577T>C	XP_016866596.1:p.Ser1193Pro
XR_002956289.1:n.3969T>C
NM_001363725.2:c.1426T>C	NP_001350654.1:p.Ser476Pro
NM_001371656.1:c.3805T>C	NP_001358585.1:p.Ser1269Pro
NM_001374820.1:c.3805T>C	NP_001361749.1:p.Ser1269Pro
NM_001374828.1:c.3925T>C MANE Select	NP_001361757.1:p.Ser1309Pro
NM_017519.3:c.3766T>C	NP_059989.3:p.Ser1256Pro