Canonical Allele Identifier: CA366228184

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3503T>A	ENSP00000055163.8:p.Leu1168Gln
ENST00000414678.8:c.3572T>A	ENSP00000412835.3:p.Leu1191Gln
ENST00000637015.2:c.3791T>A	ENSP00000489729.2:p.Leu1264Gln
ENST00000319584.11:c.1676T>A	ENSP00000313006.7:p.Leu559Gln
ENST00000346085.10:c.3542T>A	ENSP00000344546.5:p.Leu1181Gln
ENST00000350026.10:c.3254T>A	ENSP00000055163.7:p.Leu1085Gln
ENST00000414678.7:c.1820T>A	ENSP00000412835.2:p.Leu607Gln
ENST00000635849.1:c.983T>A	ENSP00000490948.1:p.Leu328Gln
ENST00000635957.1:c.617T>A	ENSP00000490385.1:p.Leu206Gln
ENST00000636930.2:c.3662T>A MANE Select	ENSP00000490491.2:p.Leu1221Gln
ENST00000636940.1:n.1659T>A
ENST00000637015.1:c.1030T>A
ENST00000637568.1:c.944T>A
ENST00000637741.1:n.328T>A
ENST00000637810.1:c.1004T>A	ENSP00000489636.1:p.Leu335Gln
ENST00000637904.1:c.1163T>A	ENSP00000490550.1:p.Leu388Gln
ENST00000647938.1:c.3293T>A	ENSP00000498155.1:p.Leu1098Gln
ENST00000319584.10:c.1679T>A	ENSP00000313006.6:p.Leu560Gln
ENST00000346085.9:c.3293T>A	ENSP00000344546.4:p.Leu1098Gln
ENST00000350026.9:c.3254T>A	ENSP00000055163.7:p.Leu1085Gln
ENST00000400790.3:c.455T>A	ENSP00000383596.3:p.Leu152Gln
ENST00000414678.6:c.1820T>A	ENSP00000412835.2:p.Leu607Gln
ENST00000478761.3:c.864T>A
NM_017519.2:c.3254T>A	NP_059989.2:p.Leu1085Gln
NM_020732.3:c.3293T>A	NP_065783.3:p.Leu1098Gln
XM_005267069.3:c.3413T>A	XP_005267126.2:p.Leu1138Gln
XM_011535984.1:c.2492T>A	XP_011534286.1:p.Leu831Gln
XM_011535985.1:c.2312T>A	XP_011534287.1:p.Leu771Gln
XM_011535986.1:c.2072T>A	XP_011534288.1:p.Leu691Gln
XM_011535987.1:c.1691T>A	XP_011534289.1:p.Leu564Gln
XM_011535988.1:c.554T>A	XP_011534290.1:p.Leu185Gln
NM_001346813.1:c.3413T>A	NP_001333742.1:p.Leu1138Gln
NM_001363725.1:c.1163T>A	NP_001350654.1:p.Leu388Gln
XM_011535984.2:c.3623T>A	XP_011534286.2:p.Leu1208Gln
XM_011535988.3:c.554T>A	XP_011534290.1:p.Leu185Gln
XM_017011103.2:c.3524T>A	XP_016866592.1:p.Leu1175Gln
XM_017011104.1:c.3494T>A	XP_016866593.1:p.Leu1165Gln
XM_017011105.2:c.3464T>A	XP_016866594.1:p.Leu1155Gln
XM_017011106.2:c.3335T>A	XP_016866595.1:p.Leu1112Gln
XM_017011107.2:c.3314T>A	XP_016866596.1:p.Leu1105Gln
XR_002956289.1:n.3706T>A
NM_001363725.2:c.1163T>A	NP_001350654.1:p.Leu388Gln
NM_001371656.1:c.3542T>A	NP_001358585.1:p.Leu1181Gln
NM_001374820.1:c.3542T>A	NP_001361749.1:p.Leu1181Gln
NM_001374828.1:c.3662T>A MANE Select	NP_001361757.1:p.Leu1221Gln
NM_017519.3:c.3503T>A	NP_059989.3:p.Leu1168Gln