Canonical Allele Identifier: CA366388613

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469763T>G (hg19) ; chr6:g.157148629T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148629T>G , CM000668.2:g.157148629T>G	GRCh38
NC_000006.11:g.157469763T>G , CM000668.1:g.157469763T>G	GRCh37
NC_000006.10:g.157511455T>G	NCBI36
NG_032093.1:g.375700T>G
NG_032093.2:g.375700T>G
NG_066624.1:g.377604T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2767T>G	ENSP00000055163.8:p.Tyr923Asp
ENST00000414678.8:c.2677T>G	ENSP00000412835.3:p.Tyr893Asp
ENST00000637015.2:c.2767T>G	ENSP00000489729.2:p.Tyr923Asp
ENST00000319584.11:c.781T>G	ENSP00000313006.7:p.Tyr261Asp
ENST00000346085.10:c.2806T>G	ENSP00000344546.5:p.Tyr936Asp
ENST00000350026.10:c.2518T>G	ENSP00000055163.7:p.Tyr840Asp
ENST00000414678.7:c.925T>G	ENSP00000412835.2:p.Tyr309Asp
ENST00000452544.2:n.668T>G
ENST00000635849.1:c.88T>G	ENSP00000490948.1:p.Tyr30Asp
ENST00000636930.2:c.2767T>G MANE Select	ENSP00000490491.2:p.Tyr923Asp
ENST00000637015.1:c.6T>G
ENST00000637810.1:c.268T>G	ENSP00000489636.1:p.Tyr90Asp
ENST00000637904.1:c.268T>G	ENSP00000490550.1:p.Tyr90Asp
ENST00000647938.1:c.2557T>G	ENSP00000498155.1:p.Tyr853Asp
ENST00000674190.1:n.1516T>G
ENST00000319584.10:c.784T>G	ENSP00000313006.6:p.Tyr262Asp
ENST00000346085.9:c.2557T>G	ENSP00000344546.4:p.Tyr853Asp
ENST00000350026.9:c.2518T>G	ENSP00000055163.7:p.Tyr840Asp
ENST00000414678.6:c.925T>G	ENSP00000412835.2:p.Tyr309Asp
ENST00000452544.1:n.614T>G
NM_017519.2:c.2518T>G	NP_059989.2:p.Tyr840Asp
NM_020732.3:c.2557T>G	NP_065783.3:p.Tyr853Asp
XM_005267069.3:c.2518T>G	XP_005267126.2:p.Tyr840Asp
XM_011535984.1:c.1468T>G	XP_011534286.1:p.Tyr490Asp
XM_011535985.1:c.1288T>G	XP_011534287.1:p.Tyr430Asp
XM_011535986.1:c.1048T>G	XP_011534288.1:p.Tyr350Asp
XM_011535987.1:c.667T>G	XP_011534289.1:p.Tyr223Asp
XM_011535988.1:c.-20+15422T>G	XP_011534290.1:n.-20+15422T>G
NM_001346813.1:c.2518T>G	NP_001333742.1:p.Tyr840Asp
NM_001363725.1:c.268T>G	NP_001350654.1:p.Tyr90Asp
XM_011535984.2:c.2599T>G	XP_011534286.2:p.Tyr867Asp
XM_011535988.3:c.-20+15422T>G	XP_011534290.1:n.-20+15422T>G
XM_017011103.2:c.2599T>G	XP_016866592.1:p.Tyr867Asp
XM_017011104.1:c.2599T>G	XP_016866593.1:p.Tyr867Asp
XM_017011105.2:c.2599T>G	XP_016866594.1:p.Tyr867Asp
XM_017011106.2:c.2599T>G	XP_016866595.1:p.Tyr867Asp
XM_017011107.2:c.2419T>G	XP_016866596.1:p.Tyr807Asp
XR_002956289.1:n.2682T>G
NM_001363725.2:c.268T>G	NP_001350654.1:p.Tyr90Asp
NM_001371656.1:c.2806T>G	NP_001358585.1:p.Tyr936Asp
NM_001374820.1:c.2806T>G	NP_001361749.1:p.Tyr936Asp
NM_001374828.1:c.2767T>G MANE Select	NP_001361757.1:p.Tyr923Asp
NM_017519.3:c.2767T>G	NP_059989.3:p.Tyr923Asp