Canonical Allele Identifier: CA366227875

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157181080-A-G
• MyVariant Identifiers: chr6:g.157502214A>G (hg19) ; chr6:g.157181080A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181080A>G , CM000668.2:g.157181080A>G	GRCh38
NC_000006.11:g.157502214A>G , CM000668.1:g.157502214A>G	GRCh37
NC_000006.10:g.157543906A>G	NCBI36
NG_032093.1:g.408151A>G
NG_032093.2:g.408151A>G
NG_066624.1:g.410055A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3457A>G	ENSP00000055163.8:p.Arg1153Gly
ENST00000414678.8:c.3526A>G	ENSP00000412835.3:p.Arg1176Gly
ENST00000637015.2:c.3745A>G	ENSP00000489729.2:p.Arg1249Gly
ENST00000319584.11:c.1630A>G	ENSP00000313006.7:p.Arg544Gly
ENST00000346085.10:c.3496A>G	ENSP00000344546.5:p.Arg1166Gly
ENST00000350026.10:c.3208A>G	ENSP00000055163.7:p.Arg1070Gly
ENST00000414678.7:c.1774A>G	ENSP00000412835.2:p.Arg592Gly
ENST00000635849.1:c.937A>G	ENSP00000490948.1:p.Arg313Gly
ENST00000635957.1:c.571A>G	ENSP00000490385.1:p.Arg191Gly
ENST00000636930.2:c.3616A>G MANE Select	ENSP00000490491.2:p.Arg1206Gly
ENST00000636940.1:n.1613A>G
ENST00000637015.1:c.984A>G
ENST00000637568.1:c.898A>G
ENST00000637741.1:n.282A>G
ENST00000637810.1:c.958A>G	ENSP00000489636.1:p.Arg320Gly
ENST00000637904.1:c.1117A>G	ENSP00000490550.1:p.Arg373Gly
ENST00000647938.1:c.3247A>G	ENSP00000498155.1:p.Arg1083Gly
ENST00000319584.10:c.1633A>G	ENSP00000313006.6:p.Arg545Gly
ENST00000346085.9:c.3247A>G	ENSP00000344546.4:p.Arg1083Gly
ENST00000350026.9:c.3208A>G	ENSP00000055163.7:p.Arg1070Gly
ENST00000400790.3:c.409A>G	ENSP00000383596.3:p.Arg137Gly
ENST00000414678.6:c.1774A>G	ENSP00000412835.2:p.Arg592Gly
ENST00000478761.3:c.818A>G
NM_017519.2:c.3208A>G	NP_059989.2:p.Arg1070Gly
NM_020732.3:c.3247A>G	NP_065783.3:p.Arg1083Gly
XM_005267069.3:c.3367A>G	XP_005267126.2:p.Arg1123Gly
XM_011535984.1:c.2446A>G	XP_011534286.1:p.Arg816Gly
XM_011535985.1:c.2266A>G	XP_011534287.1:p.Arg756Gly
XM_011535986.1:c.2026A>G	XP_011534288.1:p.Arg676Gly
XM_011535987.1:c.1645A>G	XP_011534289.1:p.Arg549Gly
XM_011535988.1:c.508A>G	XP_011534290.1:p.Arg170Gly
NM_001346813.1:c.3367A>G	NP_001333742.1:p.Arg1123Gly
NM_001363725.1:c.1117A>G	NP_001350654.1:p.Arg373Gly
XM_011535984.2:c.3577A>G	XP_011534286.2:p.Arg1193Gly
XM_011535988.3:c.508A>G	XP_011534290.1:p.Arg170Gly
XM_017011103.2:c.3478A>G	XP_016866592.1:p.Arg1160Gly
XM_017011104.1:c.3448A>G	XP_016866593.1:p.Arg1150Gly
XM_017011105.2:c.3418A>G	XP_016866594.1:p.Arg1140Gly
XM_017011106.2:c.3289A>G	XP_016866595.1:p.Arg1097Gly
XM_017011107.2:c.3268A>G	XP_016866596.1:p.Arg1090Gly
XR_002956289.1:n.3660A>G
NM_001363725.2:c.1117A>G	NP_001350654.1:p.Arg373Gly
NM_001371656.1:c.3496A>G	NP_001358585.1:p.Arg1166Gly
NM_001374820.1:c.3496A>G	NP_001361749.1:p.Arg1166Gly
NM_001374828.1:c.3616A>G MANE Select	NP_001361757.1:p.Arg1206Gly
NM_017519.3:c.3457A>G	NP_059989.3:p.Arg1153Gly