Canonical Allele Identifier: CA452990355

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469996A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148862A>G , CM000668.2:g.157148862A>G	GRCh38
NC_000006.11:g.157469996A>G , CM000668.1:g.157469996A>G	GRCh37
NC_000006.10:g.157511688A>G	NCBI36
NG_032093.1:g.375933A>G
NG_032093.2:g.375933A>G
NG_066624.1:g.377837A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3000A>G	ENSP00000055163.8:p.Gly1000=
ENST00000414678.8:c.2910A>G	ENSP00000412835.3:p.Gly970=
ENST00000637015.2:c.3000A>G	ENSP00000489729.2:p.Gly1000=
ENST00000319584.11:c.1014A>G	ENSP00000313006.7:p.Gly338=
ENST00000346085.10:c.3039A>G	ENSP00000344546.5:p.Gly1013=
ENST00000350026.10:c.2751A>G	ENSP00000055163.7:p.Gly917=
ENST00000414678.7:c.1158A>G	ENSP00000412835.2:p.Gly386=
ENST00000452544.2:n.901A>G
ENST00000635849.1:c.321A>G	ENSP00000490948.1:p.Gly107=
ENST00000636426.1:n.134A>G
ENST00000636930.2:c.3000A>G MANE Select	ENSP00000490491.2:p.Gly1000=
ENST00000637015.1:c.239A>G
ENST00000637568.1:c.43A>G
ENST00000637810.1:c.501A>G	ENSP00000489636.1:p.Gly167=
ENST00000637904.1:c.501A>G	ENSP00000490550.1:p.Gly167=
ENST00000647938.1:c.2790A>G	ENSP00000498155.1:p.Gly930=
ENST00000674190.1:n.1749A>G
ENST00000319584.10:c.1017A>G	ENSP00000313006.6:p.Gly339=
ENST00000346085.9:c.2790A>G	ENSP00000344546.4:p.Gly930=
ENST00000350026.9:c.2751A>G	ENSP00000055163.7:p.Gly917=
ENST00000414678.6:c.1158A>G	ENSP00000412835.2:p.Gly386=
ENST00000452544.1:n.847A>G
ENST00000478761.3:c.73A>G
NM_017519.2:c.2751A>G	NP_059989.2:p.Gly917=
NM_020732.3:c.2790A>G	NP_065783.3:p.Gly930=
XM_005267069.3:c.2751A>G	XP_005267126.2:p.Gly917=
XM_011535984.1:c.1701A>G	XP_011534286.1:p.Gly567=
XM_011535985.1:c.1521A>G	XP_011534287.1:p.Gly507=
XM_011535986.1:c.1281A>G	XP_011534288.1:p.Gly427=
XM_011535987.1:c.900A>G	XP_011534289.1:p.Gly300=
XM_011535988.1:c.-20+15655A>G	XP_011534290.1:n.-20+15655A>G
NM_001346813.1:c.2751A>G	NP_001333742.1:p.Gly917=
NM_001363725.1:c.501A>G	NP_001350654.1:p.Gly167=
XM_011535984.2:c.2832A>G	XP_011534286.2:p.Gly944=
XM_011535988.3:c.-20+15655A>G	XP_011534290.1:n.-20+15655A>G
XM_017011103.2:c.2832A>G	XP_016866592.1:p.Gly944=
XM_017011104.1:c.2832A>G	XP_016866593.1:p.Gly944=
XM_017011105.2:c.2832A>G	XP_016866594.1:p.Gly944=
XM_017011106.2:c.2832A>G	XP_016866595.1:p.Gly944=
XM_017011107.2:c.2652A>G	XP_016866596.1:p.Gly884=
XR_002956289.1:n.2915A>G
NM_001363725.2:c.501A>G	NP_001350654.1:p.Gly167=
NM_001371656.1:c.3039A>G	NP_001358585.1:p.Gly1013=
NM_001374820.1:c.3039A>G	NP_001361749.1:p.Gly1013=
NM_001374828.1:c.3000A>G MANE Select	NP_001361757.1:p.Gly1000=
NM_017519.3:c.3000A>G	NP_059989.3:p.Gly1000=