Canonical Allele Identifier: CA452978393

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374125
• MyVariant Identifiers: chr6:g.157522177C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201043C>G , CM000668.2:g.157201043C>G	GRCh38
NC_000006.11:g.157522177C>G , CM000668.1:g.157522177C>G	GRCh37
NC_000006.10:g.157563869C>G	NCBI36
NG_032093.1:g.428114C>G
NG_032093.2:g.428114C>G
NG_066624.1:g.430018C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4659C>G	ENSP00000055163.8:p.Gly1553=
ENST00000414678.8:c.4728C>G	ENSP00000412835.3:p.Gly1576=
ENST00000637015.2:c.4947C>G	ENSP00000489729.2:p.Gly1649=
ENST00000346085.10:c.4698C>G	ENSP00000344546.5:p.Gly1566=
ENST00000350026.10:c.4410C>G	ENSP00000055163.7:p.Gly1470=
ENST00000414678.7:c.2976C>G	ENSP00000412835.2:p.Gly992=
ENST00000635849.1:c.2139C>G	ENSP00000490948.1:p.Gly713=
ENST00000635957.1:c.1770C>G	ENSP00000490385.1:p.Gly590=
ENST00000636227.1:n.3281C>G
ENST00000636254.1:n.738C>G
ENST00000636930.2:c.4818C>G MANE Select	ENSP00000490491.2:p.Gly1606=
ENST00000636940.1:n.2815C>G
ENST00000637015.1:c.2186C>G
ENST00000637568.1:c.2100C>G
ENST00000637741.1:n.1484C>G
ENST00000637810.1:c.2160C>G	ENSP00000489636.1:p.Gly720=
ENST00000637904.1:c.2319C>G	ENSP00000490550.1:p.Gly773=
ENST00000647938.1:c.4449C>G	ENSP00000498155.1:p.Gly1483=
ENST00000346085.9:c.4449C>G	ENSP00000344546.4:p.Gly1483=
ENST00000350026.9:c.4410C>G	ENSP00000055163.7:p.Gly1470=
ENST00000414678.6:c.2976C>G	ENSP00000412835.2:p.Gly992=
NM_017519.2:c.4410C>G	NP_059989.2:p.Gly1470=
NM_020732.3:c.4449C>G	NP_065783.3:p.Gly1483=
XM_005267069.3:c.4569C>G	XP_005267126.2:p.Gly1523=
XM_011535984.1:c.3648C>G	XP_011534286.1:p.Gly1216=
XM_011535985.1:c.3468C>G	XP_011534287.1:p.Gly1156=
XM_011535986.1:c.3228C>G	XP_011534288.1:p.Gly1076=
XM_011535987.1:c.2847C>G	XP_011534289.1:p.Gly949=
XM_011535988.1:c.1710C>G	XP_011534290.1:p.Gly570=
NM_001346813.1:c.4569C>G	NP_001333742.1:p.Gly1523=
NM_001363725.1:c.2319C>G	NP_001350654.1:p.Gly773=
XM_011535984.2:c.4779C>G	XP_011534286.2:p.Gly1593=
XM_011535988.3:c.1710C>G	XP_011534290.1:p.Gly570=
XM_017011103.2:c.4680C>G	XP_016866592.1:p.Gly1560=
XM_017011104.1:c.4650C>G	XP_016866593.1:p.Gly1550=
XM_017011105.2:c.4620C>G	XP_016866594.1:p.Gly1540=
XM_017011106.2:c.4491C>G	XP_016866595.1:p.Gly1497=
XM_017011107.2:c.4470C>G	XP_016866596.1:p.Gly1490=
XR_002956289.1:n.4765C>G
NM_001363725.2:c.2319C>G	NP_001350654.1:p.Gly773=
NM_001371656.1:c.4698C>G	NP_001358585.1:p.Gly1566=
NM_001374820.1:c.4698C>G	NP_001361749.1:p.Gly1566=
NM_001374828.1:c.4818C>G MANE Select	NP_001361757.1:p.Gly1606=
NM_017519.3:c.4659C>G	NP_059989.3:p.Gly1553=