Canonical Allele Identifier: CA366388954

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469922A>G (hg19) ; chr6:g.157148788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148788A>G , CM000668.2:g.157148788A>G	GRCh38
NC_000006.11:g.157469922A>G , CM000668.1:g.157469922A>G	GRCh37
NC_000006.10:g.157511614A>G	NCBI36
NG_032093.1:g.375859A>G
NG_032093.2:g.375859A>G
NG_066624.1:g.377763A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2926A>G	ENSP00000055163.8:p.Asn976Asp
ENST00000414678.8:c.2836A>G	ENSP00000412835.3:p.Asn946Asp
ENST00000637015.2:c.2926A>G	ENSP00000489729.2:p.Asn976Asp
ENST00000319584.11:c.940A>G	ENSP00000313006.7:p.Asn314Asp
ENST00000346085.10:c.2965A>G	ENSP00000344546.5:p.Asn989Asp
ENST00000350026.10:c.2677A>G	ENSP00000055163.7:p.Asn893Asp
ENST00000414678.7:c.1084A>G	ENSP00000412835.2:p.Asn362Asp
ENST00000452544.2:n.827A>G
ENST00000635849.1:c.247A>G	ENSP00000490948.1:p.Asn83Asp
ENST00000636426.1:n.60A>G
ENST00000636930.2:c.2926A>G MANE Select	ENSP00000490491.2:p.Asn976Asp
ENST00000637015.1:c.165A>G
ENST00000637810.1:c.427A>G	ENSP00000489636.1:p.Asn143Asp
ENST00000637904.1:c.427A>G	ENSP00000490550.1:p.Asn143Asp
ENST00000647938.1:c.2716A>G	ENSP00000498155.1:p.Asn906Asp
ENST00000674190.1:n.1675A>G
ENST00000319584.10:c.943A>G	ENSP00000313006.6:p.Asn315Asp
ENST00000346085.9:c.2716A>G	ENSP00000344546.4:p.Asn906Asp
ENST00000350026.9:c.2677A>G	ENSP00000055163.7:p.Asn893Asp
ENST00000414678.6:c.1084A>G	ENSP00000412835.2:p.Asn362Asp
ENST00000452544.1:n.773A>G
NM_017519.2:c.2677A>G	NP_059989.2:p.Asn893Asp
NM_020732.3:c.2716A>G	NP_065783.3:p.Asn906Asp
XM_005267069.3:c.2677A>G	XP_005267126.2:p.Asn893Asp
XM_011535984.1:c.1627A>G	XP_011534286.1:p.Asn543Asp
XM_011535985.1:c.1447A>G	XP_011534287.1:p.Asn483Asp
XM_011535986.1:c.1207A>G	XP_011534288.1:p.Asn403Asp
XM_011535987.1:c.826A>G	XP_011534289.1:p.Asn276Asp
XM_011535988.1:c.-20+15581A>G	XP_011534290.1:n.-20+15581A>G
NM_001346813.1:c.2677A>G	NP_001333742.1:p.Asn893Asp
NM_001363725.1:c.427A>G	NP_001350654.1:p.Asn143Asp
XM_011535984.2:c.2758A>G	XP_011534286.2:p.Asn920Asp
XM_011535988.3:c.-20+15581A>G	XP_011534290.1:n.-20+15581A>G
XM_017011103.2:c.2758A>G	XP_016866592.1:p.Asn920Asp
XM_017011104.1:c.2758A>G	XP_016866593.1:p.Asn920Asp
XM_017011105.2:c.2758A>G	XP_016866594.1:p.Asn920Asp
XM_017011106.2:c.2758A>G	XP_016866595.1:p.Asn920Asp
XM_017011107.2:c.2578A>G	XP_016866596.1:p.Asn860Asp
XR_002956289.1:n.2841A>G
NM_001363725.2:c.427A>G	NP_001350654.1:p.Asn143Asp
NM_001371656.1:c.2965A>G	NP_001358585.1:p.Asn989Asp
NM_001374820.1:c.2965A>G	NP_001361749.1:p.Asn989Asp
NM_001374828.1:c.2926A>G MANE Select	NP_001361757.1:p.Asn976Asp
NM_017519.3:c.2926A>G	NP_059989.3:p.Asn976Asp