Canonical Allele Identifier: CA366388617

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148631-C-A
• MyVariant Identifiers: chr6:g.157469765C>A (hg19) ; chr6:g.157148631C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148631C>A , CM000668.2:g.157148631C>A	GRCh38
NC_000006.11:g.157469765C>A , CM000668.1:g.157469765C>A	GRCh37
NC_000006.10:g.157511457C>A	NCBI36
NG_032093.1:g.375702C>A
NG_032093.2:g.375702C>A
NG_066624.1:g.377606C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2769C>A	ENSP00000055163.8:p.Tyr923Ter
ENST00000414678.8:c.2679C>A	ENSP00000412835.3:p.Tyr893Ter
ENST00000637015.2:c.2769C>A	ENSP00000489729.2:p.Tyr923Ter
ENST00000319584.11:c.783C>A	ENSP00000313006.7:p.Tyr261Ter
ENST00000346085.10:c.2808C>A	ENSP00000344546.5:p.Tyr936Ter
ENST00000350026.10:c.2520C>A	ENSP00000055163.7:p.Tyr840Ter
ENST00000414678.7:c.927C>A	ENSP00000412835.2:p.Tyr309Ter
ENST00000452544.2:n.670C>A
ENST00000635849.1:c.90C>A	ENSP00000490948.1:p.Tyr30Ter
ENST00000636930.2:c.2769C>A MANE Select	ENSP00000490491.2:p.Tyr923Ter
ENST00000637015.1:c.8C>A
ENST00000637810.1:c.270C>A	ENSP00000489636.1:p.Tyr90Ter
ENST00000637904.1:c.270C>A	ENSP00000490550.1:p.Tyr90Ter
ENST00000647938.1:c.2559C>A	ENSP00000498155.1:p.Tyr853Ter
ENST00000674190.1:n.1518C>A
ENST00000319584.10:c.786C>A	ENSP00000313006.6:p.Tyr262Ter
ENST00000346085.9:c.2559C>A	ENSP00000344546.4:p.Tyr853Ter
ENST00000350026.9:c.2520C>A	ENSP00000055163.7:p.Tyr840Ter
ENST00000414678.6:c.927C>A	ENSP00000412835.2:p.Tyr309Ter
ENST00000452544.1:n.616C>A
NM_017519.2:c.2520C>A	NP_059989.2:p.Tyr840Ter
NM_020732.3:c.2559C>A	NP_065783.3:p.Tyr853Ter
XM_005267069.3:c.2520C>A	XP_005267126.2:p.Tyr840Ter
XM_011535984.1:c.1470C>A	XP_011534286.1:p.Tyr490Ter
XM_011535985.1:c.1290C>A	XP_011534287.1:p.Tyr430Ter
XM_011535986.1:c.1050C>A	XP_011534288.1:p.Tyr350Ter
XM_011535987.1:c.669C>A	XP_011534289.1:p.Tyr223Ter
XM_011535988.1:c.-20+15424C>A	XP_011534290.1:n.-20+15424C>A
NM_001346813.1:c.2520C>A	NP_001333742.1:p.Tyr840Ter
NM_001363725.1:c.270C>A	NP_001350654.1:p.Tyr90Ter
XM_011535984.2:c.2601C>A	XP_011534286.2:p.Tyr867Ter
XM_011535988.3:c.-20+15424C>A	XP_011534290.1:n.-20+15424C>A
XM_017011103.2:c.2601C>A	XP_016866592.1:p.Tyr867Ter
XM_017011104.1:c.2601C>A	XP_016866593.1:p.Tyr867Ter
XM_017011105.2:c.2601C>A	XP_016866594.1:p.Tyr867Ter
XM_017011106.2:c.2601C>A	XP_016866595.1:p.Tyr867Ter
XM_017011107.2:c.2421C>A	XP_016866596.1:p.Tyr807Ter
XR_002956289.1:n.2684C>A
NM_001363725.2:c.270C>A	NP_001350654.1:p.Tyr90Ter
NM_001371656.1:c.2808C>A	NP_001358585.1:p.Tyr936Ter
NM_001374820.1:c.2808C>A	NP_001361749.1:p.Tyr936Ter
NM_001374828.1:c.2769C>A MANE Select	NP_001361757.1:p.Tyr923Ter
NM_017519.3:c.2769C>A	NP_059989.3:p.Tyr923Ter