Canonical Allele Identifier: CA366228186

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502260T>G (hg19) ; chr6:g.157181126T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181126T>G , CM000668.2:g.157181126T>G	GRCh38
NC_000006.11:g.157502260T>G , CM000668.1:g.157502260T>G	GRCh37
NC_000006.10:g.157543952T>G	NCBI36
NG_032093.1:g.408197T>G
NG_032093.2:g.408197T>G
NG_066624.1:g.410101T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3503T>G	ENSP00000055163.8:p.Leu1168Arg
ENST00000414678.8:c.3572T>G	ENSP00000412835.3:p.Leu1191Arg
ENST00000637015.2:c.3791T>G	ENSP00000489729.2:p.Leu1264Arg
ENST00000319584.11:c.1676T>G	ENSP00000313006.7:p.Leu559Arg
ENST00000346085.10:c.3542T>G	ENSP00000344546.5:p.Leu1181Arg
ENST00000350026.10:c.3254T>G	ENSP00000055163.7:p.Leu1085Arg
ENST00000414678.7:c.1820T>G	ENSP00000412835.2:p.Leu607Arg
ENST00000635849.1:c.983T>G	ENSP00000490948.1:p.Leu328Arg
ENST00000635957.1:c.617T>G	ENSP00000490385.1:p.Leu206Arg
ENST00000636930.2:c.3662T>G MANE Select	ENSP00000490491.2:p.Leu1221Arg
ENST00000636940.1:n.1659T>G
ENST00000637015.1:c.1030T>G
ENST00000637568.1:c.944T>G
ENST00000637741.1:n.328T>G
ENST00000637810.1:c.1004T>G	ENSP00000489636.1:p.Leu335Arg
ENST00000637904.1:c.1163T>G	ENSP00000490550.1:p.Leu388Arg
ENST00000647938.1:c.3293T>G	ENSP00000498155.1:p.Leu1098Arg
ENST00000319584.10:c.1679T>G	ENSP00000313006.6:p.Leu560Arg
ENST00000346085.9:c.3293T>G	ENSP00000344546.4:p.Leu1098Arg
ENST00000350026.9:c.3254T>G	ENSP00000055163.7:p.Leu1085Arg
ENST00000400790.3:c.455T>G	ENSP00000383596.3:p.Leu152Arg
ENST00000414678.6:c.1820T>G	ENSP00000412835.2:p.Leu607Arg
ENST00000478761.3:c.864T>G
NM_017519.2:c.3254T>G	NP_059989.2:p.Leu1085Arg
NM_020732.3:c.3293T>G	NP_065783.3:p.Leu1098Arg
XM_005267069.3:c.3413T>G	XP_005267126.2:p.Leu1138Arg
XM_011535984.1:c.2492T>G	XP_011534286.1:p.Leu831Arg
XM_011535985.1:c.2312T>G	XP_011534287.1:p.Leu771Arg
XM_011535986.1:c.2072T>G	XP_011534288.1:p.Leu691Arg
XM_011535987.1:c.1691T>G	XP_011534289.1:p.Leu564Arg
XM_011535988.1:c.554T>G	XP_011534290.1:p.Leu185Arg
NM_001346813.1:c.3413T>G	NP_001333742.1:p.Leu1138Arg
NM_001363725.1:c.1163T>G	NP_001350654.1:p.Leu388Arg
XM_011535984.2:c.3623T>G	XP_011534286.2:p.Leu1208Arg
XM_011535988.3:c.554T>G	XP_011534290.1:p.Leu185Arg
XM_017011103.2:c.3524T>G	XP_016866592.1:p.Leu1175Arg
XM_017011104.1:c.3494T>G	XP_016866593.1:p.Leu1165Arg
XM_017011105.2:c.3464T>G	XP_016866594.1:p.Leu1155Arg
XM_017011106.2:c.3335T>G	XP_016866595.1:p.Leu1112Arg
XM_017011107.2:c.3314T>G	XP_016866596.1:p.Leu1105Arg
XR_002956289.1:n.3706T>G
NM_001363725.2:c.1163T>G	NP_001350654.1:p.Leu388Arg
NM_001371656.1:c.3542T>G	NP_001358585.1:p.Leu1181Arg
NM_001374820.1:c.3542T>G	NP_001361749.1:p.Leu1181Arg
NM_001374828.1:c.3662T>G MANE Select	NP_001361757.1:p.Leu1221Arg
NM_017519.3:c.3503T>G	NP_059989.3:p.Leu1168Arg