Canonical Allele Identifier: CA366227567

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317069
• MyVariant Identifiers: chr6:g.157502184G>T (hg19) ; chr6:g.157181050G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181050G>T , CM000668.2:g.157181050G>T	GRCh38
NC_000006.11:g.157502184G>T , CM000668.1:g.157502184G>T	GRCh37
NC_000006.10:g.157543876G>T	NCBI36
NG_032093.1:g.408121G>T
NG_032093.2:g.408121G>T
NG_066624.1:g.410025G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3427G>T	ENSP00000055163.8:p.Val1143Phe
ENST00000414678.8:c.3496G>T	ENSP00000412835.3:p.Val1166Phe
ENST00000637015.2:c.3715G>T	ENSP00000489729.2:p.Val1239Phe
ENST00000319584.11:c.1600G>T	ENSP00000313006.7:p.Val534Phe
ENST00000346085.10:c.3466G>T	ENSP00000344546.5:p.Val1156Phe
ENST00000350026.10:c.3178G>T	ENSP00000055163.7:p.Val1060Phe
ENST00000414678.7:c.1744G>T	ENSP00000412835.2:p.Val582Phe
ENST00000635849.1:c.907G>T	ENSP00000490948.1:p.Val303Phe
ENST00000635957.1:c.541G>T	ENSP00000490385.1:p.Val181Phe
ENST00000636930.2:c.3586G>T MANE Select	ENSP00000490491.2:p.Val1196Phe
ENST00000636940.1:n.1583G>T
ENST00000637015.1:c.954G>T
ENST00000637568.1:c.868G>T
ENST00000637741.1:n.252G>T
ENST00000637810.1:c.928G>T	ENSP00000489636.1:p.Val310Phe
ENST00000637904.1:c.1087G>T	ENSP00000490550.1:p.Val363Phe
ENST00000647938.1:c.3217G>T	ENSP00000498155.1:p.Val1073Phe
ENST00000319584.10:c.1603G>T	ENSP00000313006.6:p.Val535Phe
ENST00000346085.9:c.3217G>T	ENSP00000344546.4:p.Val1073Phe
ENST00000350026.9:c.3178G>T	ENSP00000055163.7:p.Val1060Phe
ENST00000400790.3:c.379G>T	ENSP00000383596.3:p.Val127Phe
ENST00000414678.6:c.1744G>T	ENSP00000412835.2:p.Val582Phe
ENST00000478761.3:c.788G>T
NM_017519.2:c.3178G>T	NP_059989.2:p.Val1060Phe
NM_020732.3:c.3217G>T	NP_065783.3:p.Val1073Phe
XM_005267069.3:c.3337G>T	XP_005267126.2:p.Val1113Phe
XM_011535984.1:c.2416G>T	XP_011534286.1:p.Val806Phe
XM_011535985.1:c.2236G>T	XP_011534287.1:p.Val746Phe
XM_011535986.1:c.1996G>T	XP_011534288.1:p.Val666Phe
XM_011535987.1:c.1615G>T	XP_011534289.1:p.Val539Phe
XM_011535988.1:c.478G>T	XP_011534290.1:p.Val160Phe
NM_001346813.1:c.3337G>T	NP_001333742.1:p.Val1113Phe
NM_001363725.1:c.1087G>T	NP_001350654.1:p.Val363Phe
XM_011535984.2:c.3547G>T	XP_011534286.2:p.Val1183Phe
XM_011535988.3:c.478G>T	XP_011534290.1:p.Val160Phe
XM_017011103.2:c.3448G>T	XP_016866592.1:p.Val1150Phe
XM_017011104.1:c.3418G>T	XP_016866593.1:p.Val1140Phe
XM_017011105.2:c.3388G>T	XP_016866594.1:p.Val1130Phe
XM_017011106.2:c.3259G>T	XP_016866595.1:p.Val1087Phe
XM_017011107.2:c.3238G>T	XP_016866596.1:p.Val1080Phe
XR_002956289.1:n.3630G>T
NM_001363725.2:c.1087G>T	NP_001350654.1:p.Val363Phe
NM_001371656.1:c.3466G>T	NP_001358585.1:p.Val1156Phe
NM_001374820.1:c.3466G>T	NP_001361749.1:p.Val1156Phe
NM_001374828.1:c.3586G>T MANE Select	NP_001361757.1:p.Val1196Phe
NM_017519.3:c.3427G>T	NP_059989.3:p.Val1143Phe