Canonical Allele Identifier: CA366388629

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469770G>T (hg19) ; chr6:g.157148636G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148636G>T , CM000668.2:g.157148636G>T	GRCh38
NC_000006.11:g.157469770G>T , CM000668.1:g.157469770G>T	GRCh37
NC_000006.10:g.157511462G>T	NCBI36
NG_032093.1:g.375707G>T
NG_032093.2:g.375707G>T
NG_066624.1:g.377611G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2774G>T	ENSP00000055163.8:p.Arg925Ile
ENST00000414678.8:c.2684G>T	ENSP00000412835.3:p.Arg895Ile
ENST00000637015.2:c.2774G>T	ENSP00000489729.2:p.Arg925Ile
ENST00000319584.11:c.788G>T	ENSP00000313006.7:p.Arg263Ile
ENST00000346085.10:c.2813G>T	ENSP00000344546.5:p.Arg938Ile
ENST00000350026.10:c.2525G>T	ENSP00000055163.7:p.Arg842Ile
ENST00000414678.7:c.932G>T	ENSP00000412835.2:p.Arg311Ile
ENST00000452544.2:n.675G>T
ENST00000635849.1:c.95G>T	ENSP00000490948.1:p.Arg32Ile
ENST00000636930.2:c.2774G>T MANE Select	ENSP00000490491.2:p.Arg925Ile
ENST00000637015.1:c.13G>T
ENST00000637810.1:c.275G>T	ENSP00000489636.1:p.Arg92Ile
ENST00000637904.1:c.275G>T	ENSP00000490550.1:p.Arg92Ile
ENST00000647938.1:c.2564G>T	ENSP00000498155.1:p.Arg855Ile
ENST00000674190.1:n.1523G>T
ENST00000319584.10:c.791G>T	ENSP00000313006.6:p.Arg264Ile
ENST00000346085.9:c.2564G>T	ENSP00000344546.4:p.Arg855Ile
ENST00000350026.9:c.2525G>T	ENSP00000055163.7:p.Arg842Ile
ENST00000414678.6:c.932G>T	ENSP00000412835.2:p.Arg311Ile
ENST00000452544.1:n.621G>T
NM_017519.2:c.2525G>T	NP_059989.2:p.Arg842Ile
NM_020732.3:c.2564G>T	NP_065783.3:p.Arg855Ile
XM_005267069.3:c.2525G>T	XP_005267126.2:p.Arg842Ile
XM_011535984.1:c.1475G>T	XP_011534286.1:p.Arg492Ile
XM_011535985.1:c.1295G>T	XP_011534287.1:p.Arg432Ile
XM_011535986.1:c.1055G>T	XP_011534288.1:p.Arg352Ile
XM_011535987.1:c.674G>T	XP_011534289.1:p.Arg225Ile
XM_011535988.1:c.-20+15429G>T	XP_011534290.1:n.-20+15429G>T
NM_001346813.1:c.2525G>T	NP_001333742.1:p.Arg842Ile
NM_001363725.1:c.275G>T	NP_001350654.1:p.Arg92Ile
XM_011535984.2:c.2606G>T	XP_011534286.2:p.Arg869Ile
XM_011535988.3:c.-20+15429G>T	XP_011534290.1:n.-20+15429G>T
XM_017011103.2:c.2606G>T	XP_016866592.1:p.Arg869Ile
XM_017011104.1:c.2606G>T	XP_016866593.1:p.Arg869Ile
XM_017011105.2:c.2606G>T	XP_016866594.1:p.Arg869Ile
XM_017011106.2:c.2606G>T	XP_016866595.1:p.Arg869Ile
XM_017011107.2:c.2426G>T	XP_016866596.1:p.Arg809Ile
XR_002956289.1:n.2689G>T
NM_001363725.2:c.275G>T	NP_001350654.1:p.Arg92Ile
NM_001371656.1:c.2813G>T	NP_001358585.1:p.Arg938Ile
NM_001374820.1:c.2813G>T	NP_001361749.1:p.Arg938Ile
NM_001374828.1:c.2774G>T MANE Select	NP_001361757.1:p.Arg925Ile
NM_017519.3:c.2774G>T	NP_059989.3:p.Arg925Ile