Canonical Allele Identifier: CA366228183

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3502C>G	ENSP00000055163.8:p.Leu1168Val
ENST00000414678.8:c.3571C>G	ENSP00000412835.3:p.Leu1191Val
ENST00000637015.2:c.3790C>G	ENSP00000489729.2:p.Leu1264Val
ENST00000319584.11:c.1675C>G	ENSP00000313006.7:p.Leu559Val
ENST00000346085.10:c.3541C>G	ENSP00000344546.5:p.Leu1181Val
ENST00000350026.10:c.3253C>G	ENSP00000055163.7:p.Leu1085Val
ENST00000414678.7:c.1819C>G	ENSP00000412835.2:p.Leu607Val
ENST00000635849.1:c.982C>G	ENSP00000490948.1:p.Leu328Val
ENST00000635957.1:c.616C>G	ENSP00000490385.1:p.Leu206Val
ENST00000636930.2:c.3661C>G MANE Select	ENSP00000490491.2:p.Leu1221Val
ENST00000636940.1:n.1658C>G
ENST00000637015.1:c.1029C>G
ENST00000637568.1:c.943C>G
ENST00000637741.1:n.327C>G
ENST00000637810.1:c.1003C>G	ENSP00000489636.1:p.Leu335Val
ENST00000637904.1:c.1162C>G	ENSP00000490550.1:p.Leu388Val
ENST00000647938.1:c.3292C>G	ENSP00000498155.1:p.Leu1098Val
ENST00000319584.10:c.1678C>G	ENSP00000313006.6:p.Leu560Val
ENST00000346085.9:c.3292C>G	ENSP00000344546.4:p.Leu1098Val
ENST00000350026.9:c.3253C>G	ENSP00000055163.7:p.Leu1085Val
ENST00000400790.3:c.454C>G	ENSP00000383596.3:p.Leu152Val
ENST00000414678.6:c.1819C>G	ENSP00000412835.2:p.Leu607Val
ENST00000478761.3:c.863C>G
NM_017519.2:c.3253C>G	NP_059989.2:p.Leu1085Val
NM_020732.3:c.3292C>G	NP_065783.3:p.Leu1098Val
XM_005267069.3:c.3412C>G	XP_005267126.2:p.Leu1138Val
XM_011535984.1:c.2491C>G	XP_011534286.1:p.Leu831Val
XM_011535985.1:c.2311C>G	XP_011534287.1:p.Leu771Val
XM_011535986.1:c.2071C>G	XP_011534288.1:p.Leu691Val
XM_011535987.1:c.1690C>G	XP_011534289.1:p.Leu564Val
XM_011535988.1:c.553C>G	XP_011534290.1:p.Leu185Val
NM_001346813.1:c.3412C>G	NP_001333742.1:p.Leu1138Val
NM_001363725.1:c.1162C>G	NP_001350654.1:p.Leu388Val
XM_011535984.2:c.3622C>G	XP_011534286.2:p.Leu1208Val
XM_011535988.3:c.553C>G	XP_011534290.1:p.Leu185Val
XM_017011103.2:c.3523C>G	XP_016866592.1:p.Leu1175Val
XM_017011104.1:c.3493C>G	XP_016866593.1:p.Leu1165Val
XM_017011105.2:c.3463C>G	XP_016866594.1:p.Leu1155Val
XM_017011106.2:c.3334C>G	XP_016866595.1:p.Leu1112Val
XM_017011107.2:c.3313C>G	XP_016866596.1:p.Leu1105Val
XR_002956289.1:n.3705C>G
NM_001363725.2:c.1162C>G	NP_001350654.1:p.Leu388Val
NM_001371656.1:c.3541C>G	NP_001358585.1:p.Leu1181Val
NM_001374820.1:c.3541C>G	NP_001361749.1:p.Leu1181Val
NM_001374828.1:c.3661C>G MANE Select	NP_001361757.1:p.Leu1221Val
NM_017519.3:c.3502C>G	NP_059989.3:p.Leu1168Val