Canonical Allele Identifier: CA366227852

Gene: ARID1B

Linked Data

• dbSNP Id: rs766340916
• MyVariant Identifiers: chr6:g.157502211G>T (hg19) ; chr6:g.157181077G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181077G>T , CM000668.2:g.157181077G>T	GRCh38
NC_000006.11:g.157502211G>T , CM000668.1:g.157502211G>T	GRCh37
NC_000006.10:g.157543903G>T	NCBI36
NG_032093.1:g.408148G>T
NG_032093.2:g.408148G>T
NG_066624.1:g.410052G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3454G>T	ENSP00000055163.8:p.Glu1152Ter
ENST00000414678.8:c.3523G>T	ENSP00000412835.3:p.Glu1175Ter
ENST00000637015.2:c.3742G>T	ENSP00000489729.2:p.Glu1248Ter
ENST00000319584.11:c.1627G>T	ENSP00000313006.7:p.Glu543Ter
ENST00000346085.10:c.3493G>T	ENSP00000344546.5:p.Glu1165Ter
ENST00000350026.10:c.3205G>T	ENSP00000055163.7:p.Glu1069Ter
ENST00000414678.7:c.1771G>T	ENSP00000412835.2:p.Glu591Ter
ENST00000635849.1:c.934G>T	ENSP00000490948.1:p.Glu312Ter
ENST00000635957.1:c.568G>T	ENSP00000490385.1:p.Glu190Ter
ENST00000636930.2:c.3613G>T MANE Select	ENSP00000490491.2:p.Glu1205Ter
ENST00000636940.1:n.1610G>T
ENST00000637015.1:c.981G>T
ENST00000637568.1:c.895G>T
ENST00000637741.1:n.279G>T
ENST00000637810.1:c.955G>T	ENSP00000489636.1:p.Glu319Ter
ENST00000637904.1:c.1114G>T	ENSP00000490550.1:p.Glu372Ter
ENST00000647938.1:c.3244G>T	ENSP00000498155.1:p.Glu1082Ter
ENST00000319584.10:c.1630G>T	ENSP00000313006.6:p.Glu544Ter
ENST00000346085.9:c.3244G>T	ENSP00000344546.4:p.Glu1082Ter
ENST00000350026.9:c.3205G>T	ENSP00000055163.7:p.Glu1069Ter
ENST00000400790.3:c.406G>T	ENSP00000383596.3:p.Glu136Ter
ENST00000414678.6:c.1771G>T	ENSP00000412835.2:p.Glu591Ter
ENST00000478761.3:c.815G>T
NM_017519.2:c.3205G>T	NP_059989.2:p.Glu1069Ter
NM_020732.3:c.3244G>T	NP_065783.3:p.Glu1082Ter
XM_005267069.3:c.3364G>T	XP_005267126.2:p.Glu1122Ter
XM_011535984.1:c.2443G>T	XP_011534286.1:p.Glu815Ter
XM_011535985.1:c.2263G>T	XP_011534287.1:p.Glu755Ter
XM_011535986.1:c.2023G>T	XP_011534288.1:p.Glu675Ter
XM_011535987.1:c.1642G>T	XP_011534289.1:p.Glu548Ter
XM_011535988.1:c.505G>T	XP_011534290.1:p.Glu169Ter
NM_001346813.1:c.3364G>T	NP_001333742.1:p.Glu1122Ter
NM_001363725.1:c.1114G>T	NP_001350654.1:p.Glu372Ter
XM_011535984.2:c.3574G>T	XP_011534286.2:p.Glu1192Ter
XM_011535988.3:c.505G>T	XP_011534290.1:p.Glu169Ter
XM_017011103.2:c.3475G>T	XP_016866592.1:p.Glu1159Ter
XM_017011104.1:c.3445G>T	XP_016866593.1:p.Glu1149Ter
XM_017011105.2:c.3415G>T	XP_016866594.1:p.Glu1139Ter
XM_017011106.2:c.3286G>T	XP_016866595.1:p.Glu1096Ter
XM_017011107.2:c.3265G>T	XP_016866596.1:p.Glu1089Ter
XR_002956289.1:n.3657G>T
NM_001363725.2:c.1114G>T	NP_001350654.1:p.Glu372Ter
NM_001371656.1:c.3493G>T	NP_001358585.1:p.Glu1165Ter
NM_001374820.1:c.3493G>T	NP_001361749.1:p.Glu1165Ter
NM_001374828.1:c.3613G>T MANE Select	NP_001361757.1:p.Glu1205Ter
NM_017519.3:c.3454G>T	NP_059989.3:p.Glu1152Ter