Canonical Allele Identifier: CA452978298

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201298-T-G
• MyVariant Identifiers: chr6:g.157522432T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201298T>G , CM000668.2:g.157201298T>G	GRCh38
NC_000006.11:g.157522432T>G , CM000668.1:g.157522432T>G	GRCh37
NC_000006.10:g.157564124T>G	NCBI36
NG_032093.1:g.428369T>G
NG_032093.2:g.428369T>G
NG_066624.1:g.430273T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4914T>G	ENSP00000055163.8:p.Ser1638=
ENST00000414678.8:c.4983T>G	ENSP00000412835.3:p.Ser1661=
ENST00000637015.2:c.5202T>G	ENSP00000489729.2:p.Ser1734=
ENST00000346085.10:c.4953T>G	ENSP00000344546.5:p.Ser1651=
ENST00000350026.10:c.4665T>G	ENSP00000055163.7:p.Ser1555=
ENST00000414678.7:c.3231T>G	ENSP00000412835.2:p.Ser1077=
ENST00000635849.1:c.2394T>G	ENSP00000490948.1:p.Ser798=
ENST00000635957.1:c.2025T>G	ENSP00000490385.1:p.Ser675=
ENST00000636227.1:n.3536T>G
ENST00000636254.1:n.993T>G
ENST00000636930.2:c.5073T>G MANE Select	ENSP00000490491.2:p.Ser1691=
ENST00000636940.1:n.3070T>G
ENST00000637015.1:c.2441T>G
ENST00000637568.1:c.2355T>G
ENST00000637741.1:n.1739T>G
ENST00000637810.1:c.2415T>G	ENSP00000489636.1:p.Ser805=
ENST00000637904.1:c.2574T>G	ENSP00000490550.1:p.Ser858=
ENST00000647938.1:c.4704T>G	ENSP00000498155.1:p.Ser1568=
ENST00000346085.9:c.4704T>G	ENSP00000344546.4:p.Ser1568=
ENST00000350026.9:c.4665T>G	ENSP00000055163.7:p.Ser1555=
ENST00000414678.6:c.3231T>G	ENSP00000412835.2:p.Ser1077=
NM_017519.2:c.4665T>G	NP_059989.2:p.Ser1555=
NM_020732.3:c.4704T>G	NP_065783.3:p.Ser1568=
XM_005267069.3:c.4824T>G	XP_005267126.2:p.Ser1608=
XM_011535984.1:c.3903T>G	XP_011534286.1:p.Ser1301=
XM_011535985.1:c.3723T>G	XP_011534287.1:p.Ser1241=
XM_011535986.1:c.3483T>G	XP_011534288.1:p.Ser1161=
XM_011535987.1:c.3102T>G	XP_011534289.1:p.Ser1034=
XM_011535988.1:c.1965T>G	XP_011534290.1:p.Ser655=
NM_001346813.1:c.4824T>G	NP_001333742.1:p.Ser1608=
NM_001363725.1:c.2574T>G	NP_001350654.1:p.Ser858=
XM_011535984.2:c.5034T>G	XP_011534286.2:p.Ser1678=
XM_011535988.3:c.1965T>G	XP_011534290.1:p.Ser655=
XM_017011103.2:c.4935T>G	XP_016866592.1:p.Ser1645=
XM_017011104.1:c.4905T>G	XP_016866593.1:p.Ser1635=
XM_017011105.2:c.4875T>G	XP_016866594.1:p.Ser1625=
XM_017011106.2:c.4746T>G	XP_016866595.1:p.Ser1582=
XM_017011107.2:c.4725T>G	XP_016866596.1:p.Ser1575=
XR_002956289.1:n.5020T>G
NM_001363725.2:c.2574T>G	NP_001350654.1:p.Ser858=
NM_001371656.1:c.4953T>G	NP_001358585.1:p.Ser1651=
NM_001374820.1:c.4953T>G	NP_001361749.1:p.Ser1651=
NM_001374828.1:c.5073T>G MANE Select	NP_001361757.1:p.Ser1691=
NM_017519.3:c.4914T>G	NP_059989.3:p.Ser1638=