Canonical Allele Identifier: CA366242392

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522412T>G (hg19) ; chr6:g.157201278T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4894T>G	ENSP00000055163.8:p.Ser1632Ala
ENST00000414678.8:c.4963T>G	ENSP00000412835.3:p.Ser1655Ala
ENST00000637015.2:c.5182T>G	ENSP00000489729.2:p.Ser1728Ala
ENST00000346085.10:c.4933T>G	ENSP00000344546.5:p.Ser1645Ala
ENST00000350026.10:c.4645T>G	ENSP00000055163.7:p.Ser1549Ala
ENST00000414678.7:c.3211T>G	ENSP00000412835.2:p.Ser1071Ala
ENST00000635849.1:c.2374T>G	ENSP00000490948.1:p.Ser792Ala
ENST00000635957.1:c.2005T>G	ENSP00000490385.1:p.Ser669Ala
ENST00000636227.1:n.3516T>G
ENST00000636254.1:n.973T>G
ENST00000636930.2:c.5053T>G MANE Select	ENSP00000490491.2:p.Ser1685Ala
ENST00000636940.1:n.3050T>G
ENST00000637015.1:c.2421T>G
ENST00000637568.1:c.2335T>G
ENST00000637741.1:n.1719T>G
ENST00000637810.1:c.2395T>G	ENSP00000489636.1:p.Ser799Ala
ENST00000637904.1:c.2554T>G	ENSP00000490550.1:p.Ser852Ala
ENST00000647938.1:c.4684T>G	ENSP00000498155.1:p.Ser1562Ala
ENST00000346085.9:c.4684T>G	ENSP00000344546.4:p.Ser1562Ala
ENST00000350026.9:c.4645T>G	ENSP00000055163.7:p.Ser1549Ala
ENST00000414678.6:c.3211T>G	ENSP00000412835.2:p.Ser1071Ala
NM_017519.2:c.4645T>G	NP_059989.2:p.Ser1549Ala
NM_020732.3:c.4684T>G	NP_065783.3:p.Ser1562Ala
XM_005267069.3:c.4804T>G	XP_005267126.2:p.Ser1602Ala
XM_011535984.1:c.3883T>G	XP_011534286.1:p.Ser1295Ala
XM_011535985.1:c.3703T>G	XP_011534287.1:p.Ser1235Ala
XM_011535986.1:c.3463T>G	XP_011534288.1:p.Ser1155Ala
XM_011535987.1:c.3082T>G	XP_011534289.1:p.Ser1028Ala
XM_011535988.1:c.1945T>G	XP_011534290.1:p.Ser649Ala
NM_001346813.1:c.4804T>G	NP_001333742.1:p.Ser1602Ala
NM_001363725.1:c.2554T>G	NP_001350654.1:p.Ser852Ala
XM_011535984.2:c.5014T>G	XP_011534286.2:p.Ser1672Ala
XM_011535988.3:c.1945T>G	XP_011534290.1:p.Ser649Ala
XM_017011103.2:c.4915T>G	XP_016866592.1:p.Ser1639Ala
XM_017011104.1:c.4885T>G	XP_016866593.1:p.Ser1629Ala
XM_017011105.2:c.4855T>G	XP_016866594.1:p.Ser1619Ala
XM_017011106.2:c.4726T>G	XP_016866595.1:p.Ser1576Ala
XM_017011107.2:c.4705T>G	XP_016866596.1:p.Ser1569Ala
XR_002956289.1:n.5000T>G
NM_001363725.2:c.2554T>G	NP_001350654.1:p.Ser852Ala
NM_001371656.1:c.4933T>G	NP_001358585.1:p.Ser1645Ala
NM_001374820.1:c.4933T>G	NP_001361749.1:p.Ser1645Ala
NM_001374828.1:c.5053T>G MANE Select	NP_001361757.1:p.Ser1685Ala
NM_017519.3:c.4894T>G	NP_059989.3:p.Ser1632Ala