Canonical Allele Identifier: CA366234366

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554232979
• MyVariant Identifiers: chr6:g.157510904C>T (hg19) ; chr6:g.157189770C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189770C>T , CM000668.2:g.157189770C>T	GRCh38
NC_000006.11:g.157510904C>T , CM000668.1:g.157510904C>T	GRCh37
NC_000006.10:g.157552596C>T	NCBI36
NG_032093.1:g.416841C>T
NG_032093.2:g.416841C>T
NG_066624.1:g.418745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3889C>T	ENSP00000055163.8:p.Gln1297Ter
ENST00000414678.8:c.3958C>T	ENSP00000412835.3:p.Gln1320Ter
ENST00000637015.2:c.4177C>T	ENSP00000489729.2:p.Gln1393Ter
ENST00000346085.10:c.3928C>T	ENSP00000344546.5:p.Gln1310Ter
ENST00000350026.10:c.3640C>T	ENSP00000055163.7:p.Gln1214Ter
ENST00000414678.7:c.2206C>T	ENSP00000412835.2:p.Gln736Ter
ENST00000635849.1:c.1369C>T	ENSP00000490948.1:p.Gln457Ter
ENST00000635957.1:c.1003C>T	ENSP00000490385.1:p.Gln335Ter
ENST00000636930.2:c.4048C>T MANE Select	ENSP00000490491.2:p.Gln1350Ter
ENST00000636940.1:n.2045C>T
ENST00000637015.1:c.1416C>T
ENST00000637568.1:c.1330C>T
ENST00000637741.1:n.714C>T
ENST00000637810.1:c.1390C>T	ENSP00000489636.1:p.Gln464Ter
ENST00000637904.1:c.1549C>T	ENSP00000490550.1:p.Gln517Ter
ENST00000647938.1:c.3679C>T	ENSP00000498155.1:p.Gln1227Ter
ENST00000346085.9:c.3679C>T	ENSP00000344546.4:p.Gln1227Ter
ENST00000350026.9:c.3640C>T	ENSP00000055163.7:p.Gln1214Ter
ENST00000414678.6:c.2206C>T	ENSP00000412835.2:p.Gln736Ter
NM_017519.2:c.3640C>T	NP_059989.2:p.Gln1214Ter
NM_020732.3:c.3679C>T	NP_065783.3:p.Gln1227Ter
XM_005267069.3:c.3799C>T	XP_005267126.2:p.Gln1267Ter
XM_011535984.1:c.2878C>T	XP_011534286.1:p.Gln960Ter
XM_011535985.1:c.2698C>T	XP_011534287.1:p.Gln900Ter
XM_011535986.1:c.2458C>T	XP_011534288.1:p.Gln820Ter
XM_011535987.1:c.2077C>T	XP_011534289.1:p.Gln693Ter
XM_011535988.1:c.940C>T	XP_011534290.1:p.Gln314Ter
NM_001346813.1:c.3799C>T	NP_001333742.1:p.Gln1267Ter
NM_001363725.1:c.1549C>T	NP_001350654.1:p.Gln517Ter
XM_011535984.2:c.4009C>T	XP_011534286.2:p.Gln1337Ter
XM_011535988.3:c.940C>T	XP_011534290.1:p.Gln314Ter
XM_017011103.2:c.3910C>T	XP_016866592.1:p.Gln1304Ter
XM_017011104.1:c.3880C>T	XP_016866593.1:p.Gln1294Ter
XM_017011105.2:c.3850C>T	XP_016866594.1:p.Gln1284Ter
XM_017011106.2:c.3721C>T	XP_016866595.1:p.Gln1241Ter
XM_017011107.2:c.3700C>T	XP_016866596.1:p.Gln1234Ter
XR_002956289.1:n.4092C>T
NM_001363725.2:c.1549C>T	NP_001350654.1:p.Gln517Ter
NM_001371656.1:c.3928C>T	NP_001358585.1:p.Gln1310Ter
NM_001374820.1:c.3928C>T	NP_001361749.1:p.Gln1310Ter
NM_001374828.1:c.4048C>T MANE Select	NP_001361757.1:p.Gln1350Ter
NM_017519.3:c.3889C>T	NP_059989.3:p.Gln1297Ter