Canonical Allele Identifier: CA366235273

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190103-A-G
• MyVariant Identifiers: chr6:g.157511237A>G (hg19) ; chr6:g.157190103A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190103A>G , CM000668.2:g.157190103A>G	GRCh38
NC_000006.11:g.157511237A>G , CM000668.1:g.157511237A>G	GRCh37
NC_000006.10:g.157552929A>G	NCBI36
NG_032093.1:g.417174A>G
NG_032093.2:g.417174A>G
NG_066624.1:g.419078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3965A>G	ENSP00000055163.8:p.Asn1322Ser
ENST00000414678.8:c.4034A>G	ENSP00000412835.3:p.Asn1345Ser
ENST00000637015.2:c.4253A>G	ENSP00000489729.2:p.Asn1418Ser
ENST00000346085.10:c.4004A>G	ENSP00000344546.5:p.Asn1335Ser
ENST00000350026.10:c.3716A>G	ENSP00000055163.7:p.Asn1239Ser
ENST00000414678.7:c.2282A>G	ENSP00000412835.2:p.Asn761Ser
ENST00000635849.1:c.1445A>G	ENSP00000490948.1:p.Asn482Ser
ENST00000635957.1:c.1076A>G	ENSP00000490385.1:p.Asn359Ser
ENST00000636930.2:c.4124A>G MANE Select	ENSP00000490491.2:p.Asn1375Ser
ENST00000636940.1:n.2121A>G
ENST00000637015.1:c.1492A>G
ENST00000637568.1:c.1406A>G
ENST00000637741.1:n.790A>G
ENST00000637810.1:c.1466A>G	ENSP00000489636.1:p.Asn489Ser
ENST00000637904.1:c.1625A>G	ENSP00000490550.1:p.Asn542Ser
ENST00000647938.1:c.3755A>G	ENSP00000498155.1:p.Asn1252Ser
ENST00000346085.9:c.3755A>G	ENSP00000344546.4:p.Asn1252Ser
ENST00000350026.9:c.3716A>G	ENSP00000055163.7:p.Asn1239Ser
ENST00000414678.6:c.2282A>G	ENSP00000412835.2:p.Asn761Ser
NM_017519.2:c.3716A>G	NP_059989.2:p.Asn1239Ser
NM_020732.3:c.3755A>G	NP_065783.3:p.Asn1252Ser
XM_005267069.3:c.3875A>G	XP_005267126.2:p.Asn1292Ser
XM_011535984.1:c.2954A>G	XP_011534286.1:p.Asn985Ser
XM_011535985.1:c.2774A>G	XP_011534287.1:p.Asn925Ser
XM_011535986.1:c.2534A>G	XP_011534288.1:p.Asn845Ser
XM_011535987.1:c.2153A>G	XP_011534289.1:p.Asn718Ser
XM_011535988.1:c.1016A>G	XP_011534290.1:p.Asn339Ser
NM_001346813.1:c.3875A>G	NP_001333742.1:p.Asn1292Ser
NM_001363725.1:c.1625A>G	NP_001350654.1:p.Asn542Ser
XM_011535984.2:c.4085A>G	XP_011534286.2:p.Asn1362Ser
XM_011535988.3:c.1016A>G	XP_011534290.1:p.Asn339Ser
XM_017011103.2:c.3986A>G	XP_016866592.1:p.Asn1329Ser
XM_017011104.1:c.3956A>G	XP_016866593.1:p.Asn1319Ser
XM_017011105.2:c.3926A>G	XP_016866594.1:p.Asn1309Ser
XM_017011106.2:c.3797A>G	XP_016866595.1:p.Asn1266Ser
XM_017011107.2:c.3776A>G	XP_016866596.1:p.Asn1259Ser
XR_002956289.1:n.4168A>G
NM_001363725.2:c.1625A>G	NP_001350654.1:p.Asn542Ser
NM_001371656.1:c.4004A>G	NP_001358585.1:p.Asn1335Ser
NM_001374820.1:c.4004A>G	NP_001361749.1:p.Asn1335Ser
NM_001374828.1:c.4124A>G MANE Select	NP_001361757.1:p.Asn1375Ser
NM_017519.3:c.3965A>G	NP_059989.3:p.Asn1322Ser