Canonical Allele Identifier: CA150362517

Gene: ARID1B

Linked Data

• dbSNP Id: rs902679026
• gnomAD v2: 6-157510830-C-T
• gnomAD v3: 6-157189696-C-T
• gnomAD v4: 6-157189696-C-T
• COSMIC: COSM5607845 ; COSM5607846
• MyVariant Identifiers: chr6:g.157510830C>T (hg19) ; chr6:g.157189696C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189696C>T , CM000668.2:g.157189696C>T	GRCh38
NC_000006.11:g.157510830C>T , CM000668.1:g.157510830C>T	GRCh37
NC_000006.10:g.157552522C>T	NCBI36
NG_032093.1:g.416767C>T
NG_032093.2:g.416767C>T
NG_066624.1:g.418671C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3815C>T	ENSP00000055163.8:p.Ser1272Phe
ENST00000414678.8:c.3884C>T	ENSP00000412835.3:p.Ser1295Phe
ENST00000637015.2:c.4103C>T	ENSP00000489729.2:p.Ser1368Phe
ENST00000346085.10:c.3854C>T	ENSP00000344546.5:p.Ser1285Phe
ENST00000350026.10:c.3566C>T	ENSP00000055163.7:p.Ser1189Phe
ENST00000414678.7:c.2132C>T	ENSP00000412835.2:p.Ser711Phe
ENST00000635849.1:c.1295C>T	ENSP00000490948.1:p.Ser432Phe
ENST00000635957.1:c.929C>T	ENSP00000490385.1:p.Ser310Phe
ENST00000636930.2:c.3974C>T MANE Select	ENSP00000490491.2:p.Ser1325Phe
ENST00000636940.1:n.1971C>T
ENST00000637015.1:c.1342C>T
ENST00000637568.1:c.1256C>T
ENST00000637741.1:n.640C>T
ENST00000637810.1:c.1316C>T	ENSP00000489636.1:p.Ser439Phe
ENST00000637904.1:c.1475C>T	ENSP00000490550.1:p.Ser492Phe
ENST00000647938.1:c.3605C>T	ENSP00000498155.1:p.Ser1202Phe
ENST00000346085.9:c.3605C>T	ENSP00000344546.4:p.Ser1202Phe
ENST00000350026.9:c.3566C>T	ENSP00000055163.7:p.Ser1189Phe
ENST00000414678.6:c.2132C>T	ENSP00000412835.2:p.Ser711Phe
NM_017519.2:c.3566C>T	NP_059989.2:p.Ser1189Phe
NM_020732.3:c.3605C>T	NP_065783.3:p.Ser1202Phe
XM_005267069.3:c.3725C>T	XP_005267126.2:p.Ser1242Phe
XM_011535984.1:c.2804C>T	XP_011534286.1:p.Ser935Phe
XM_011535985.1:c.2624C>T	XP_011534287.1:p.Ser875Phe
XM_011535986.1:c.2384C>T	XP_011534288.1:p.Ser795Phe
XM_011535987.1:c.2003C>T	XP_011534289.1:p.Ser668Phe
XM_011535988.1:c.866C>T	XP_011534290.1:p.Ser289Phe
NM_001346813.1:c.3725C>T	NP_001333742.1:p.Ser1242Phe
NM_001363725.1:c.1475C>T	NP_001350654.1:p.Ser492Phe
XM_011535984.2:c.3935C>T	XP_011534286.2:p.Ser1312Phe
XM_011535988.3:c.866C>T	XP_011534290.1:p.Ser289Phe
XM_017011103.2:c.3836C>T	XP_016866592.1:p.Ser1279Phe
XM_017011104.1:c.3806C>T	XP_016866593.1:p.Ser1269Phe
XM_017011105.2:c.3776C>T	XP_016866594.1:p.Ser1259Phe
XM_017011106.2:c.3647C>T	XP_016866595.1:p.Ser1216Phe
XM_017011107.2:c.3626C>T	XP_016866596.1:p.Ser1209Phe
XR_002956289.1:n.4018C>T
NM_001363725.2:c.1475C>T	NP_001350654.1:p.Ser492Phe
NM_001371656.1:c.3854C>T	NP_001358585.1:p.Ser1285Phe
NM_001374820.1:c.3854C>T	NP_001361749.1:p.Ser1285Phe
NM_001374828.1:c.3974C>T MANE Select	NP_001361757.1:p.Ser1325Phe
NM_017519.3:c.3815C>T	NP_059989.3:p.Ser1272Phe