Canonical Allele Identifier: CA366228182

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317558
• MyVariant Identifiers: chr6:g.157502259C>A (hg19) ; chr6:g.157181125C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181125C>A , CM000668.2:g.157181125C>A	GRCh38
NC_000006.11:g.157502259C>A , CM000668.1:g.157502259C>A	GRCh37
NC_000006.10:g.157543951C>A	NCBI36
NG_032093.1:g.408196C>A
NG_032093.2:g.408196C>A
NG_066624.1:g.410100C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3502C>A	ENSP00000055163.8:p.Leu1168Met
ENST00000414678.8:c.3571C>A	ENSP00000412835.3:p.Leu1191Met
ENST00000637015.2:c.3790C>A	ENSP00000489729.2:p.Leu1264Met
ENST00000319584.11:c.1675C>A	ENSP00000313006.7:p.Leu559Met
ENST00000346085.10:c.3541C>A	ENSP00000344546.5:p.Leu1181Met
ENST00000350026.10:c.3253C>A	ENSP00000055163.7:p.Leu1085Met
ENST00000414678.7:c.1819C>A	ENSP00000412835.2:p.Leu607Met
ENST00000635849.1:c.982C>A	ENSP00000490948.1:p.Leu328Met
ENST00000635957.1:c.616C>A	ENSP00000490385.1:p.Leu206Met
ENST00000636930.2:c.3661C>A MANE Select	ENSP00000490491.2:p.Leu1221Met
ENST00000636940.1:n.1658C>A
ENST00000637015.1:c.1029C>A
ENST00000637568.1:c.943C>A
ENST00000637741.1:n.327C>A
ENST00000637810.1:c.1003C>A	ENSP00000489636.1:p.Leu335Met
ENST00000637904.1:c.1162C>A	ENSP00000490550.1:p.Leu388Met
ENST00000647938.1:c.3292C>A	ENSP00000498155.1:p.Leu1098Met
ENST00000319584.10:c.1678C>A	ENSP00000313006.6:p.Leu560Met
ENST00000346085.9:c.3292C>A	ENSP00000344546.4:p.Leu1098Met
ENST00000350026.9:c.3253C>A	ENSP00000055163.7:p.Leu1085Met
ENST00000400790.3:c.454C>A	ENSP00000383596.3:p.Leu152Met
ENST00000414678.6:c.1819C>A	ENSP00000412835.2:p.Leu607Met
ENST00000478761.3:c.863C>A
NM_017519.2:c.3253C>A	NP_059989.2:p.Leu1085Met
NM_020732.3:c.3292C>A	NP_065783.3:p.Leu1098Met
XM_005267069.3:c.3412C>A	XP_005267126.2:p.Leu1138Met
XM_011535984.1:c.2491C>A	XP_011534286.1:p.Leu831Met
XM_011535985.1:c.2311C>A	XP_011534287.1:p.Leu771Met
XM_011535986.1:c.2071C>A	XP_011534288.1:p.Leu691Met
XM_011535987.1:c.1690C>A	XP_011534289.1:p.Leu564Met
XM_011535988.1:c.553C>A	XP_011534290.1:p.Leu185Met
NM_001346813.1:c.3412C>A	NP_001333742.1:p.Leu1138Met
NM_001363725.1:c.1162C>A	NP_001350654.1:p.Leu388Met
XM_011535984.2:c.3622C>A	XP_011534286.2:p.Leu1208Met
XM_011535988.3:c.553C>A	XP_011534290.1:p.Leu185Met
XM_017011103.2:c.3523C>A	XP_016866592.1:p.Leu1175Met
XM_017011104.1:c.3493C>A	XP_016866593.1:p.Leu1165Met
XM_017011105.2:c.3463C>A	XP_016866594.1:p.Leu1155Met
XM_017011106.2:c.3334C>A	XP_016866595.1:p.Leu1112Met
XM_017011107.2:c.3313C>A	XP_016866596.1:p.Leu1105Met
XR_002956289.1:n.3705C>A
NM_001363725.2:c.1162C>A	NP_001350654.1:p.Leu388Met
NM_001371656.1:c.3541C>A	NP_001358585.1:p.Leu1181Met
NM_001374820.1:c.3541C>A	NP_001361749.1:p.Leu1181Met
NM_001374828.1:c.3661C>A MANE Select	NP_001361757.1:p.Leu1221Met
NM_017519.3:c.3502C>A	NP_059989.3:p.Leu1168Met