Canonical Allele Identifier: CA366241323

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522099T>A (hg19) ; chr6:g.157200965T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200965T>A , CM000668.2:g.157200965T>A	GRCh38
NC_000006.11:g.157522099T>A , CM000668.1:g.157522099T>A	GRCh37
NC_000006.10:g.157563791T>A	NCBI36
NG_032093.1:g.428036T>A
NG_032093.2:g.428036T>A
NG_066624.1:g.429940T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4581T>A	ENSP00000055163.8:p.Ser1527Arg
ENST00000414678.8:c.4650T>A	ENSP00000412835.3:p.Ser1550Arg
ENST00000637015.2:c.4869T>A	ENSP00000489729.2:p.Ser1623Arg
ENST00000346085.10:c.4620T>A	ENSP00000344546.5:p.Ser1540Arg
ENST00000350026.10:c.4332T>A	ENSP00000055163.7:p.Ser1444Arg
ENST00000414678.7:c.2898T>A	ENSP00000412835.2:p.Ser966Arg
ENST00000635849.1:c.2061T>A	ENSP00000490948.1:p.Ser687Arg
ENST00000635957.1:c.1692T>A	ENSP00000490385.1:p.Ser564Arg
ENST00000636227.1:n.3203T>A
ENST00000636254.1:n.660T>A
ENST00000636930.2:c.4740T>A MANE Select	ENSP00000490491.2:p.Ser1580Arg
ENST00000636940.1:n.2737T>A
ENST00000637015.1:c.2108T>A
ENST00000637568.1:c.2022T>A
ENST00000637741.1:n.1406T>A
ENST00000637810.1:c.2082T>A	ENSP00000489636.1:p.Ser694Arg
ENST00000637904.1:c.2241T>A	ENSP00000490550.1:p.Ser747Arg
ENST00000647938.1:c.4371T>A	ENSP00000498155.1:p.Ser1457Arg
ENST00000346085.9:c.4371T>A	ENSP00000344546.4:p.Ser1457Arg
ENST00000350026.9:c.4332T>A	ENSP00000055163.7:p.Ser1444Arg
ENST00000414678.6:c.2898T>A	ENSP00000412835.2:p.Ser966Arg
NM_017519.2:c.4332T>A	NP_059989.2:p.Ser1444Arg
NM_020732.3:c.4371T>A	NP_065783.3:p.Ser1457Arg
XM_005267069.3:c.4491T>A	XP_005267126.2:p.Ser1497Arg
XM_011535984.1:c.3570T>A	XP_011534286.1:p.Ser1190Arg
XM_011535985.1:c.3390T>A	XP_011534287.1:p.Ser1130Arg
XM_011535986.1:c.3150T>A	XP_011534288.1:p.Ser1050Arg
XM_011535987.1:c.2769T>A	XP_011534289.1:p.Ser923Arg
XM_011535988.1:c.1632T>A	XP_011534290.1:p.Ser544Arg
NM_001346813.1:c.4491T>A	NP_001333742.1:p.Ser1497Arg
NM_001363725.1:c.2241T>A	NP_001350654.1:p.Ser747Arg
XM_011535984.2:c.4701T>A	XP_011534286.2:p.Ser1567Arg
XM_011535988.3:c.1632T>A	XP_011534290.1:p.Ser544Arg
XM_017011103.2:c.4602T>A	XP_016866592.1:p.Ser1534Arg
XM_017011104.1:c.4572T>A	XP_016866593.1:p.Ser1524Arg
XM_017011105.2:c.4542T>A	XP_016866594.1:p.Ser1514Arg
XM_017011106.2:c.4413T>A	XP_016866595.1:p.Ser1471Arg
XM_017011107.2:c.4392T>A	XP_016866596.1:p.Ser1464Arg
XR_002956289.1:n.4687T>A
NM_001363725.2:c.2241T>A	NP_001350654.1:p.Ser747Arg
NM_001371656.1:c.4620T>A	NP_001358585.1:p.Ser1540Arg
NM_001374820.1:c.4620T>A	NP_001361749.1:p.Ser1540Arg
NM_001374828.1:c.4740T>A MANE Select	NP_001361757.1:p.Ser1580Arg
NM_017519.3:c.4581T>A	NP_059989.3:p.Ser1527Arg