Canonical Allele Identifier: CA366241986

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522233C>G (hg19) ; chr6:g.157201099C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201099C>G , CM000668.2:g.157201099C>G	GRCh38
NC_000006.11:g.157522233C>G , CM000668.1:g.157522233C>G	GRCh37
NC_000006.10:g.157563925C>G	NCBI36
NG_032093.1:g.428170C>G
NG_032093.2:g.428170C>G
NG_066624.1:g.430074C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4715C>G	ENSP00000055163.8:p.Pro1572Arg
ENST00000414678.8:c.4784C>G	ENSP00000412835.3:p.Pro1595Arg
ENST00000637015.2:c.5003C>G	ENSP00000489729.2:p.Pro1668Arg
ENST00000346085.10:c.4754C>G	ENSP00000344546.5:p.Pro1585Arg
ENST00000350026.10:c.4466C>G	ENSP00000055163.7:p.Pro1489Arg
ENST00000414678.7:c.3032C>G	ENSP00000412835.2:p.Pro1011Arg
ENST00000635849.1:c.2195C>G	ENSP00000490948.1:p.Pro732Arg
ENST00000635957.1:c.1826C>G	ENSP00000490385.1:p.Pro609Arg
ENST00000636227.1:n.3337C>G
ENST00000636254.1:n.794C>G
ENST00000636930.2:c.4874C>G MANE Select	ENSP00000490491.2:p.Pro1625Arg
ENST00000636940.1:n.2871C>G
ENST00000637015.1:c.2242C>G
ENST00000637568.1:c.2156C>G
ENST00000637741.1:n.1540C>G
ENST00000637810.1:c.2216C>G	ENSP00000489636.1:p.Pro739Arg
ENST00000637904.1:c.2375C>G	ENSP00000490550.1:p.Pro792Arg
ENST00000647938.1:c.4505C>G	ENSP00000498155.1:p.Pro1502Arg
ENST00000346085.9:c.4505C>G	ENSP00000344546.4:p.Pro1502Arg
ENST00000350026.9:c.4466C>G	ENSP00000055163.7:p.Pro1489Arg
ENST00000414678.6:c.3032C>G	ENSP00000412835.2:p.Pro1011Arg
NM_017519.2:c.4466C>G	NP_059989.2:p.Pro1489Arg
NM_020732.3:c.4505C>G	NP_065783.3:p.Pro1502Arg
XM_005267069.3:c.4625C>G	XP_005267126.2:p.Pro1542Arg
XM_011535984.1:c.3704C>G	XP_011534286.1:p.Pro1235Arg
XM_011535985.1:c.3524C>G	XP_011534287.1:p.Pro1175Arg
XM_011535986.1:c.3284C>G	XP_011534288.1:p.Pro1095Arg
XM_011535987.1:c.2903C>G	XP_011534289.1:p.Pro968Arg
XM_011535988.1:c.1766C>G	XP_011534290.1:p.Pro589Arg
NM_001346813.1:c.4625C>G	NP_001333742.1:p.Pro1542Arg
NM_001363725.1:c.2375C>G	NP_001350654.1:p.Pro792Arg
XM_011535984.2:c.4835C>G	XP_011534286.2:p.Pro1612Arg
XM_011535988.3:c.1766C>G	XP_011534290.1:p.Pro589Arg
XM_017011103.2:c.4736C>G	XP_016866592.1:p.Pro1579Arg
XM_017011104.1:c.4706C>G	XP_016866593.1:p.Pro1569Arg
XM_017011105.2:c.4676C>G	XP_016866594.1:p.Pro1559Arg
XM_017011106.2:c.4547C>G	XP_016866595.1:p.Pro1516Arg
XM_017011107.2:c.4526C>G	XP_016866596.1:p.Pro1509Arg
XR_002956289.1:n.4821C>G
NM_001363725.2:c.2375C>G	NP_001350654.1:p.Pro792Arg
NM_001371656.1:c.4754C>G	NP_001358585.1:p.Pro1585Arg
NM_001374820.1:c.4754C>G	NP_001361749.1:p.Pro1585Arg
NM_001374828.1:c.4874C>G MANE Select	NP_001361757.1:p.Pro1625Arg
NM_017519.3:c.4715C>G	NP_059989.3:p.Pro1572Arg