Canonical Allele Identifier: CA366242390

Gene: ARID1B

Linked Data

• dbSNP Id: rs1317545135
• MyVariant Identifiers: chr6:g.157522412T>A (hg19) ; chr6:g.157201278T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201278T>A , CM000668.2:g.157201278T>A	GRCh38
NC_000006.11:g.157522412T>A , CM000668.1:g.157522412T>A	GRCh37
NC_000006.10:g.157564104T>A	NCBI36
NG_032093.1:g.428349T>A
NG_032093.2:g.428349T>A
NG_066624.1:g.430253T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4894T>A	ENSP00000055163.8:p.Ser1632Thr
ENST00000414678.8:c.4963T>A	ENSP00000412835.3:p.Ser1655Thr
ENST00000637015.2:c.5182T>A	ENSP00000489729.2:p.Ser1728Thr
ENST00000346085.10:c.4933T>A	ENSP00000344546.5:p.Ser1645Thr
ENST00000350026.10:c.4645T>A	ENSP00000055163.7:p.Ser1549Thr
ENST00000414678.7:c.3211T>A	ENSP00000412835.2:p.Ser1071Thr
ENST00000635849.1:c.2374T>A	ENSP00000490948.1:p.Ser792Thr
ENST00000635957.1:c.2005T>A	ENSP00000490385.1:p.Ser669Thr
ENST00000636227.1:n.3516T>A
ENST00000636254.1:n.973T>A
ENST00000636930.2:c.5053T>A MANE Select	ENSP00000490491.2:p.Ser1685Thr
ENST00000636940.1:n.3050T>A
ENST00000637015.1:c.2421T>A
ENST00000637568.1:c.2335T>A
ENST00000637741.1:n.1719T>A
ENST00000637810.1:c.2395T>A	ENSP00000489636.1:p.Ser799Thr
ENST00000637904.1:c.2554T>A	ENSP00000490550.1:p.Ser852Thr
ENST00000647938.1:c.4684T>A	ENSP00000498155.1:p.Ser1562Thr
ENST00000346085.9:c.4684T>A	ENSP00000344546.4:p.Ser1562Thr
ENST00000350026.9:c.4645T>A	ENSP00000055163.7:p.Ser1549Thr
ENST00000414678.6:c.3211T>A	ENSP00000412835.2:p.Ser1071Thr
NM_017519.2:c.4645T>A	NP_059989.2:p.Ser1549Thr
NM_020732.3:c.4684T>A	NP_065783.3:p.Ser1562Thr
XM_005267069.3:c.4804T>A	XP_005267126.2:p.Ser1602Thr
XM_011535984.1:c.3883T>A	XP_011534286.1:p.Ser1295Thr
XM_011535985.1:c.3703T>A	XP_011534287.1:p.Ser1235Thr
XM_011535986.1:c.3463T>A	XP_011534288.1:p.Ser1155Thr
XM_011535987.1:c.3082T>A	XP_011534289.1:p.Ser1028Thr
XM_011535988.1:c.1945T>A	XP_011534290.1:p.Ser649Thr
NM_001346813.1:c.4804T>A	NP_001333742.1:p.Ser1602Thr
NM_001363725.1:c.2554T>A	NP_001350654.1:p.Ser852Thr
XM_011535984.2:c.5014T>A	XP_011534286.2:p.Ser1672Thr
XM_011535988.3:c.1945T>A	XP_011534290.1:p.Ser649Thr
XM_017011103.2:c.4915T>A	XP_016866592.1:p.Ser1639Thr
XM_017011104.1:c.4885T>A	XP_016866593.1:p.Ser1629Thr
XM_017011105.2:c.4855T>A	XP_016866594.1:p.Ser1619Thr
XM_017011106.2:c.4726T>A	XP_016866595.1:p.Ser1576Thr
XM_017011107.2:c.4705T>A	XP_016866596.1:p.Ser1569Thr
XR_002956289.1:n.5000T>A
NM_001363725.2:c.2554T>A	NP_001350654.1:p.Ser852Thr
NM_001371656.1:c.4933T>A	NP_001358585.1:p.Ser1645Thr
NM_001374820.1:c.4933T>A	NP_001361749.1:p.Ser1645Thr
NM_001374828.1:c.5053T>A MANE Select	NP_001361757.1:p.Ser1685Thr
NM_017519.3:c.4894T>A	NP_059989.3:p.Ser1632Thr