Canonical Allele Identifier: CA366246174

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157527519G>T (hg19) ; chr6:g.157206385G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206385G>T , CM000668.2:g.157206385G>T	GRCh38
NC_000006.11:g.157527519G>T , CM000668.1:g.157527519G>T	GRCh37
NC_000006.10:g.157569211G>T	NCBI36
NG_032093.1:g.433456G>T
NG_032093.2:g.433456G>T
NG_066624.1:g.435360G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.5454G>T	ENSP00000055163.8:p.Glu1818Asp
ENST00000414678.8:c.5523G>T	ENSP00000412835.3:p.Glu1841Asp
ENST00000637015.2:c.5742G>T	ENSP00000489729.2:p.Glu1914Asp
ENST00000346085.10:c.5493G>T	ENSP00000344546.5:p.Glu1831Asp
ENST00000350026.10:c.5205G>T	ENSP00000055163.7:p.Glu1735Asp
ENST00000414678.7:c.3771G>T	ENSP00000412835.2:p.Glu1257Asp
ENST00000635849.1:c.2934G>T	ENSP00000490948.1:p.Glu978Asp
ENST00000635957.1:c.2565G>T	ENSP00000490385.1:p.Glu855Asp
ENST00000636227.1:n.4076G>T
ENST00000636254.1:n.1533G>T
ENST00000636930.2:c.5613G>T MANE Select	ENSP00000490491.2:p.Glu1871Asp
ENST00000636940.1:n.3610G>T
ENST00000637015.1:c.2981G>T
ENST00000637568.1:c.2895G>T
ENST00000637741.1:n.2279G>T
ENST00000637810.1:c.2955G>T	ENSP00000489636.1:p.Glu985Asp
ENST00000637904.1:c.3114G>T	ENSP00000490550.1:p.Glu1038Asp
ENST00000637933.1:n.2728G>T
ENST00000647938.1:c.5244G>T	ENSP00000498155.1:p.Glu1748Asp
ENST00000346085.9:c.5244G>T	ENSP00000344546.4:p.Glu1748Asp
ENST00000350026.9:c.5205G>T	ENSP00000055163.7:p.Glu1735Asp
ENST00000414678.6:c.3771G>T	ENSP00000412835.2:p.Glu1257Asp
NM_017519.2:c.5205G>T	NP_059989.2:p.Glu1735Asp
NM_020732.3:c.5244G>T	NP_065783.3:p.Glu1748Asp
XM_005267069.3:c.5364G>T	XP_005267126.2:p.Glu1788Asp
XM_011535984.1:c.4443G>T	XP_011534286.1:p.Glu1481Asp
XM_011535985.1:c.4263G>T	XP_011534287.1:p.Glu1421Asp
XM_011535986.1:c.4023G>T	XP_011534288.1:p.Glu1341Asp
XM_011535987.1:c.3642G>T	XP_011534289.1:p.Glu1214Asp
XM_011535988.1:c.2505G>T	XP_011534290.1:p.Glu835Asp
NM_001346813.1:c.5364G>T	NP_001333742.1:p.Glu1788Asp
NM_001363725.1:c.3114G>T	NP_001350654.1:p.Glu1038Asp
XM_011535984.2:c.5574G>T	XP_011534286.2:p.Glu1858Asp
XM_011535988.3:c.2505G>T	XP_011534290.1:p.Glu835Asp
XM_017011103.2:c.5475G>T	XP_016866592.1:p.Glu1825Asp
XM_017011104.1:c.5445G>T	XP_016866593.1:p.Glu1815Asp
XM_017011105.2:c.5415G>T	XP_016866594.1:p.Glu1805Asp
XM_017011106.2:c.5286G>T	XP_016866595.1:p.Glu1762Asp
XM_017011107.2:c.5265G>T	XP_016866596.1:p.Glu1755Asp
XR_002956289.1:n.5560G>T
NM_001363725.2:c.3114G>T	NP_001350654.1:p.Glu1038Asp
NM_001371656.1:c.5493G>T	NP_001358585.1:p.Glu1831Asp
NM_001374820.1:c.5493G>T	NP_001361749.1:p.Glu1831Asp
NM_001374828.1:c.5613G>T MANE Select	NP_001361757.1:p.Glu1871Asp
NM_017519.3:c.5454G>T	NP_059989.3:p.Glu1818Asp