Canonical Allele Identifier: CA366227491

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231202
• gnomAD v4: 6-157181041-A-G
• MyVariant Identifiers: chr6:g.157502175A>G (hg19) ; chr6:g.157181041A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181041A>G , CM000668.2:g.157181041A>G	GRCh38
NC_000006.11:g.157502175A>G , CM000668.1:g.157502175A>G	GRCh37
NC_000006.10:g.157543867A>G	NCBI36
NG_032093.1:g.408112A>G
NG_032093.2:g.408112A>G
NG_066624.1:g.410016A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3418A>G	ENSP00000055163.8:p.Lys1140Glu
ENST00000414678.8:c.3487A>G	ENSP00000412835.3:p.Lys1163Glu
ENST00000637015.2:c.3706A>G	ENSP00000489729.2:p.Lys1236Glu
ENST00000319584.11:c.1591A>G	ENSP00000313006.7:p.Lys531Glu
ENST00000346085.10:c.3457A>G	ENSP00000344546.5:p.Lys1153Glu
ENST00000350026.10:c.3169A>G	ENSP00000055163.7:p.Lys1057Glu
ENST00000414678.7:c.1735A>G	ENSP00000412835.2:p.Lys579Glu
ENST00000635849.1:c.898A>G	ENSP00000490948.1:p.Lys300Glu
ENST00000635957.1:c.532A>G	ENSP00000490385.1:p.Lys178Glu
ENST00000636930.2:c.3577A>G MANE Select	ENSP00000490491.2:p.Lys1193Glu
ENST00000636940.1:n.1574A>G
ENST00000637015.1:c.945A>G
ENST00000637568.1:c.859A>G
ENST00000637741.1:n.243A>G
ENST00000637810.1:c.919A>G	ENSP00000489636.1:p.Lys307Glu
ENST00000637904.1:c.1078A>G	ENSP00000490550.1:p.Lys360Glu
ENST00000647938.1:c.3208A>G	ENSP00000498155.1:p.Lys1070Glu
ENST00000319584.10:c.1594A>G	ENSP00000313006.6:p.Lys532Glu
ENST00000346085.9:c.3208A>G	ENSP00000344546.4:p.Lys1070Glu
ENST00000350026.9:c.3169A>G	ENSP00000055163.7:p.Lys1057Glu
ENST00000400790.3:c.370A>G	ENSP00000383596.3:p.Lys124Glu
ENST00000414678.6:c.1735A>G	ENSP00000412835.2:p.Lys579Glu
ENST00000478761.3:c.779A>G
NM_017519.2:c.3169A>G	NP_059989.2:p.Lys1057Glu
NM_020732.3:c.3208A>G	NP_065783.3:p.Lys1070Glu
XM_005267069.3:c.3328A>G	XP_005267126.2:p.Lys1110Glu
XM_011535984.1:c.2407A>G	XP_011534286.1:p.Lys803Glu
XM_011535985.1:c.2227A>G	XP_011534287.1:p.Lys743Glu
XM_011535986.1:c.1987A>G	XP_011534288.1:p.Lys663Glu
XM_011535987.1:c.1606A>G	XP_011534289.1:p.Lys536Glu
XM_011535988.1:c.469A>G	XP_011534290.1:p.Lys157Glu
NM_001346813.1:c.3328A>G	NP_001333742.1:p.Lys1110Glu
NM_001363725.1:c.1078A>G	NP_001350654.1:p.Lys360Glu
XM_011535984.2:c.3538A>G	XP_011534286.2:p.Lys1180Glu
XM_011535988.3:c.469A>G	XP_011534290.1:p.Lys157Glu
XM_017011103.2:c.3439A>G	XP_016866592.1:p.Lys1147Glu
XM_017011104.1:c.3409A>G	XP_016866593.1:p.Lys1137Glu
XM_017011105.2:c.3379A>G	XP_016866594.1:p.Lys1127Glu
XM_017011106.2:c.3250A>G	XP_016866595.1:p.Lys1084Glu
XM_017011107.2:c.3229A>G	XP_016866596.1:p.Lys1077Glu
XR_002956289.1:n.3621A>G
NM_001363725.2:c.1078A>G	NP_001350654.1:p.Lys360Glu
NM_001371656.1:c.3457A>G	NP_001358585.1:p.Lys1153Glu
NM_001374820.1:c.3457A>G	NP_001361749.1:p.Lys1153Glu
NM_001374828.1:c.3577A>G MANE Select	NP_001361757.1:p.Lys1193Glu
NM_017519.3:c.3418A>G	NP_059989.3:p.Lys1140Glu