Canonical Allele Identifier: CA366242348

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201258-G-T
• MyVariant Identifiers: chr6:g.157522392G>T (hg19) ; chr6:g.157201258G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201258G>T , CM000668.2:g.157201258G>T	GRCh38
NC_000006.11:g.157522392G>T , CM000668.1:g.157522392G>T	GRCh37
NC_000006.10:g.157564084G>T	NCBI36
NG_032093.1:g.428329G>T
NG_032093.2:g.428329G>T
NG_066624.1:g.430233G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4874G>T	ENSP00000055163.8:p.Ser1625Ile
ENST00000414678.8:c.4943G>T	ENSP00000412835.3:p.Ser1648Ile
ENST00000637015.2:c.5162G>T	ENSP00000489729.2:p.Ser1721Ile
ENST00000346085.10:c.4913G>T	ENSP00000344546.5:p.Ser1638Ile
ENST00000350026.10:c.4625G>T	ENSP00000055163.7:p.Ser1542Ile
ENST00000414678.7:c.3191G>T	ENSP00000412835.2:p.Ser1064Ile
ENST00000635849.1:c.2354G>T	ENSP00000490948.1:p.Ser785Ile
ENST00000635957.1:c.1985G>T	ENSP00000490385.1:p.Ser662Ile
ENST00000636227.1:n.3496G>T
ENST00000636254.1:n.953G>T
ENST00000636930.2:c.5033G>T MANE Select	ENSP00000490491.2:p.Ser1678Ile
ENST00000636940.1:n.3030G>T
ENST00000637015.1:c.2401G>T
ENST00000637568.1:c.2315G>T
ENST00000637741.1:n.1699G>T
ENST00000637810.1:c.2375G>T	ENSP00000489636.1:p.Ser792Ile
ENST00000637904.1:c.2534G>T	ENSP00000490550.1:p.Ser845Ile
ENST00000647938.1:c.4664G>T	ENSP00000498155.1:p.Ser1555Ile
ENST00000346085.9:c.4664G>T	ENSP00000344546.4:p.Ser1555Ile
ENST00000350026.9:c.4625G>T	ENSP00000055163.7:p.Ser1542Ile
ENST00000414678.6:c.3191G>T	ENSP00000412835.2:p.Ser1064Ile
NM_017519.2:c.4625G>T	NP_059989.2:p.Ser1542Ile
NM_020732.3:c.4664G>T	NP_065783.3:p.Ser1555Ile
XM_005267069.3:c.4784G>T	XP_005267126.2:p.Ser1595Ile
XM_011535984.1:c.3863G>T	XP_011534286.1:p.Ser1288Ile
XM_011535985.1:c.3683G>T	XP_011534287.1:p.Ser1228Ile
XM_011535986.1:c.3443G>T	XP_011534288.1:p.Ser1148Ile
XM_011535987.1:c.3062G>T	XP_011534289.1:p.Ser1021Ile
XM_011535988.1:c.1925G>T	XP_011534290.1:p.Ser642Ile
NM_001346813.1:c.4784G>T	NP_001333742.1:p.Ser1595Ile
NM_001363725.1:c.2534G>T	NP_001350654.1:p.Ser845Ile
XM_011535984.2:c.4994G>T	XP_011534286.2:p.Ser1665Ile
XM_011535988.3:c.1925G>T	XP_011534290.1:p.Ser642Ile
XM_017011103.2:c.4895G>T	XP_016866592.1:p.Ser1632Ile
XM_017011104.1:c.4865G>T	XP_016866593.1:p.Ser1622Ile
XM_017011105.2:c.4835G>T	XP_016866594.1:p.Ser1612Ile
XM_017011106.2:c.4706G>T	XP_016866595.1:p.Ser1569Ile
XM_017011107.2:c.4685G>T	XP_016866596.1:p.Ser1562Ile
XR_002956289.1:n.4980G>T
NM_001363725.2:c.2534G>T	NP_001350654.1:p.Ser845Ile
NM_001371656.1:c.4913G>T	NP_001358585.1:p.Ser1638Ile
NM_001374820.1:c.4913G>T	NP_001361749.1:p.Ser1638Ile
NM_001374828.1:c.5033G>T MANE Select	NP_001361757.1:p.Ser1678Ile
NM_017519.3:c.4874G>T	NP_059989.3:p.Ser1625Ile