Canonical Allele Identifier: CA366228577

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502312G>T (hg19) ; chr6:g.157181178G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181178G>T , CM000668.2:g.157181178G>T	GRCh38
NC_000006.11:g.157502312G>T , CM000668.1:g.157502312G>T	GRCh37
NC_000006.10:g.157544004G>T	NCBI36
NG_032093.1:g.408249G>T
NG_032093.2:g.408249G>T
NG_066624.1:g.410153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3555G>T	ENSP00000055163.8:p.Gln1185His
ENST00000414678.8:c.3624G>T	ENSP00000412835.3:p.Gln1208His
ENST00000637015.2:c.3843G>T	ENSP00000489729.2:p.Gln1281His
ENST00000319584.11:c.1728G>T	ENSP00000313006.7:p.Gln576His
ENST00000346085.10:c.3594G>T	ENSP00000344546.5:p.Gln1198His
ENST00000350026.10:c.3306G>T	ENSP00000055163.7:p.Gln1102His
ENST00000414678.7:c.1872G>T	ENSP00000412835.2:p.Gln624His
ENST00000635849.1:c.1035G>T	ENSP00000490948.1:p.Gln345His
ENST00000635957.1:c.669G>T	ENSP00000490385.1:p.Gln223His
ENST00000636930.2:c.3714G>T MANE Select	ENSP00000490491.2:p.Gln1238His
ENST00000636940.1:n.1711G>T
ENST00000637015.1:c.1082G>T
ENST00000637568.1:c.996G>T
ENST00000637741.1:n.380G>T
ENST00000637810.1:c.1056G>T	ENSP00000489636.1:p.Gln352His
ENST00000637904.1:c.1215G>T	ENSP00000490550.1:p.Gln405His
ENST00000647938.1:c.3345G>T	ENSP00000498155.1:p.Gln1115His
ENST00000319584.10:c.1731G>T	ENSP00000313006.6:p.Gln577His
ENST00000346085.9:c.3345G>T	ENSP00000344546.4:p.Gln1115His
ENST00000350026.9:c.3306G>T	ENSP00000055163.7:p.Gln1102His
ENST00000400790.3:c.507G>T	ENSP00000383596.3:p.Gln169His
ENST00000414678.6:c.1872G>T	ENSP00000412835.2:p.Gln624His
ENST00000478761.3:c.916G>T
NM_017519.2:c.3306G>T	NP_059989.2:p.Gln1102His
NM_020732.3:c.3345G>T	NP_065783.3:p.Gln1115His
XM_005267069.3:c.3465G>T	XP_005267126.2:p.Gln1155His
XM_011535984.1:c.2544G>T	XP_011534286.1:p.Gln848His
XM_011535985.1:c.2364G>T	XP_011534287.1:p.Gln788His
XM_011535986.1:c.2124G>T	XP_011534288.1:p.Gln708His
XM_011535987.1:c.1743G>T	XP_011534289.1:p.Gln581His
XM_011535988.1:c.606G>T	XP_011534290.1:p.Gln202His
NM_001346813.1:c.3465G>T	NP_001333742.1:p.Gln1155His
NM_001363725.1:c.1215G>T	NP_001350654.1:p.Gln405His
XM_011535984.2:c.3675G>T	XP_011534286.2:p.Gln1225His
XM_011535988.3:c.606G>T	XP_011534290.1:p.Gln202His
XM_017011103.2:c.3576G>T	XP_016866592.1:p.Gln1192His
XM_017011104.1:c.3546G>T	XP_016866593.1:p.Gln1182His
XM_017011105.2:c.3516G>T	XP_016866594.1:p.Gln1172His
XM_017011106.2:c.3387G>T	XP_016866595.1:p.Gln1129His
XM_017011107.2:c.3366G>T	XP_016866596.1:p.Gln1122His
XR_002956289.1:n.3758G>T
NM_001363725.2:c.1215G>T	NP_001350654.1:p.Gln405His
NM_001371656.1:c.3594G>T	NP_001358585.1:p.Gln1198His
NM_001374820.1:c.3594G>T	NP_001361749.1:p.Gln1198His
NM_001374828.1:c.3714G>T MANE Select	NP_001361757.1:p.Gln1238His
NM_017519.3:c.3555G>T	NP_059989.3:p.Gln1185His