Canonical Allele Identifier: CA366389032

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469955A>G (hg19) ; chr6:g.157148821A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148821A>G , CM000668.2:g.157148821A>G	GRCh38
NC_000006.11:g.157469955A>G , CM000668.1:g.157469955A>G	GRCh37
NC_000006.10:g.157511647A>G	NCBI36
NG_032093.1:g.375892A>G
NG_032093.2:g.375892A>G
NG_066624.1:g.377796A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2959A>G	ENSP00000055163.8:p.Thr987Ala
ENST00000414678.8:c.2869A>G	ENSP00000412835.3:p.Thr957Ala
ENST00000637015.2:c.2959A>G	ENSP00000489729.2:p.Thr987Ala
ENST00000319584.11:c.973A>G	ENSP00000313006.7:p.Thr325Ala
ENST00000346085.10:c.2998A>G	ENSP00000344546.5:p.Thr1000Ala
ENST00000350026.10:c.2710A>G	ENSP00000055163.7:p.Thr904Ala
ENST00000414678.7:c.1117A>G	ENSP00000412835.2:p.Thr373Ala
ENST00000452544.2:n.860A>G
ENST00000635849.1:c.280A>G	ENSP00000490948.1:p.Thr94Ala
ENST00000636426.1:n.93A>G
ENST00000636930.2:c.2959A>G MANE Select	ENSP00000490491.2:p.Thr987Ala
ENST00000637015.1:c.198A>G
ENST00000637568.1:c.2A>G
ENST00000637810.1:c.460A>G	ENSP00000489636.1:p.Thr154Ala
ENST00000637904.1:c.460A>G	ENSP00000490550.1:p.Thr154Ala
ENST00000647938.1:c.2749A>G	ENSP00000498155.1:p.Thr917Ala
ENST00000674190.1:n.1708A>G
ENST00000319584.10:c.976A>G	ENSP00000313006.6:p.Thr326Ala
ENST00000346085.9:c.2749A>G	ENSP00000344546.4:p.Thr917Ala
ENST00000350026.9:c.2710A>G	ENSP00000055163.7:p.Thr904Ala
ENST00000414678.6:c.1117A>G	ENSP00000412835.2:p.Thr373Ala
ENST00000452544.1:n.806A>G
ENST00000478761.3:c.32A>G
NM_017519.2:c.2710A>G	NP_059989.2:p.Thr904Ala
NM_020732.3:c.2749A>G	NP_065783.3:p.Thr917Ala
XM_005267069.3:c.2710A>G	XP_005267126.2:p.Thr904Ala
XM_011535984.1:c.1660A>G	XP_011534286.1:p.Thr554Ala
XM_011535985.1:c.1480A>G	XP_011534287.1:p.Thr494Ala
XM_011535986.1:c.1240A>G	XP_011534288.1:p.Thr414Ala
XM_011535987.1:c.859A>G	XP_011534289.1:p.Thr287Ala
XM_011535988.1:c.-20+15614A>G	XP_011534290.1:n.-20+15614A>G
NM_001346813.1:c.2710A>G	NP_001333742.1:p.Thr904Ala
NM_001363725.1:c.460A>G	NP_001350654.1:p.Thr154Ala
XM_011535984.2:c.2791A>G	XP_011534286.2:p.Thr931Ala
XM_011535988.3:c.-20+15614A>G	XP_011534290.1:n.-20+15614A>G
XM_017011103.2:c.2791A>G	XP_016866592.1:p.Thr931Ala
XM_017011104.1:c.2791A>G	XP_016866593.1:p.Thr931Ala
XM_017011105.2:c.2791A>G	XP_016866594.1:p.Thr931Ala
XM_017011106.2:c.2791A>G	XP_016866595.1:p.Thr931Ala
XM_017011107.2:c.2611A>G	XP_016866596.1:p.Thr871Ala
XR_002956289.1:n.2874A>G
NM_001363725.2:c.460A>G	NP_001350654.1:p.Thr154Ala
NM_001371656.1:c.2998A>G	NP_001358585.1:p.Thr1000Ala
NM_001374820.1:c.2998A>G	NP_001361749.1:p.Thr1000Ala
NM_001374828.1:c.2959A>G MANE Select	NP_001361757.1:p.Thr987Ala
NM_017519.3:c.2959A>G	NP_059989.3:p.Thr987Ala