Canonical Allele Identifier: CA366228281

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502274C>G (hg19) ; chr6:g.157181140C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181140C>G , CM000668.2:g.157181140C>G	GRCh38
NC_000006.11:g.157502274C>G , CM000668.1:g.157502274C>G	GRCh37
NC_000006.10:g.157543966C>G	NCBI36
NG_032093.1:g.408211C>G
NG_032093.2:g.408211C>G
NG_066624.1:g.410115C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3517C>G	ENSP00000055163.8:p.Leu1173Val
ENST00000414678.8:c.3586C>G	ENSP00000412835.3:p.Leu1196Val
ENST00000637015.2:c.3805C>G	ENSP00000489729.2:p.Leu1269Val
ENST00000319584.11:c.1690C>G	ENSP00000313006.7:p.Leu564Val
ENST00000346085.10:c.3556C>G	ENSP00000344546.5:p.Leu1186Val
ENST00000350026.10:c.3268C>G	ENSP00000055163.7:p.Leu1090Val
ENST00000414678.7:c.1834C>G	ENSP00000412835.2:p.Leu612Val
ENST00000635849.1:c.997C>G	ENSP00000490948.1:p.Leu333Val
ENST00000635957.1:c.631C>G	ENSP00000490385.1:p.Leu211Val
ENST00000636930.2:c.3676C>G MANE Select	ENSP00000490491.2:p.Leu1226Val
ENST00000636940.1:n.1673C>G
ENST00000637015.1:c.1044C>G
ENST00000637568.1:c.958C>G
ENST00000637741.1:n.342C>G
ENST00000637810.1:c.1018C>G	ENSP00000489636.1:p.Leu340Val
ENST00000637904.1:c.1177C>G	ENSP00000490550.1:p.Leu393Val
ENST00000647938.1:c.3307C>G	ENSP00000498155.1:p.Leu1103Val
ENST00000319584.10:c.1693C>G	ENSP00000313006.6:p.Leu565Val
ENST00000346085.9:c.3307C>G	ENSP00000344546.4:p.Leu1103Val
ENST00000350026.9:c.3268C>G	ENSP00000055163.7:p.Leu1090Val
ENST00000400790.3:c.469C>G	ENSP00000383596.3:p.Leu157Val
ENST00000414678.6:c.1834C>G	ENSP00000412835.2:p.Leu612Val
ENST00000478761.3:c.878C>G
NM_017519.2:c.3268C>G	NP_059989.2:p.Leu1090Val
NM_020732.3:c.3307C>G	NP_065783.3:p.Leu1103Val
XM_005267069.3:c.3427C>G	XP_005267126.2:p.Leu1143Val
XM_011535984.1:c.2506C>G	XP_011534286.1:p.Leu836Val
XM_011535985.1:c.2326C>G	XP_011534287.1:p.Leu776Val
XM_011535986.1:c.2086C>G	XP_011534288.1:p.Leu696Val
XM_011535987.1:c.1705C>G	XP_011534289.1:p.Leu569Val
XM_011535988.1:c.568C>G	XP_011534290.1:p.Leu190Val
NM_001346813.1:c.3427C>G	NP_001333742.1:p.Leu1143Val
NM_001363725.1:c.1177C>G	NP_001350654.1:p.Leu393Val
XM_011535984.2:c.3637C>G	XP_011534286.2:p.Leu1213Val
XM_011535988.3:c.568C>G	XP_011534290.1:p.Leu190Val
XM_017011103.2:c.3538C>G	XP_016866592.1:p.Leu1180Val
XM_017011104.1:c.3508C>G	XP_016866593.1:p.Leu1170Val
XM_017011105.2:c.3478C>G	XP_016866594.1:p.Leu1160Val
XM_017011106.2:c.3349C>G	XP_016866595.1:p.Leu1117Val
XM_017011107.2:c.3328C>G	XP_016866596.1:p.Leu1110Val
XR_002956289.1:n.3720C>G
NM_001363725.2:c.1177C>G	NP_001350654.1:p.Leu393Val
NM_001371656.1:c.3556C>G	NP_001358585.1:p.Leu1186Val
NM_001374820.1:c.3556C>G	NP_001361749.1:p.Leu1186Val
NM_001374828.1:c.3676C>G MANE Select	NP_001361757.1:p.Leu1226Val
NM_017519.3:c.3517C>G	NP_059989.3:p.Leu1173Val