Canonical Allele Identifier: CA366228176

Gene: ARID1B

Linked Data

• dbSNP Id: rs1387977593
• MyVariant Identifiers: chr6:g.157502257C>G (hg19) ; chr6:g.157181123C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181123C>G , CM000668.2:g.157181123C>G	GRCh38
NC_000006.11:g.157502257C>G , CM000668.1:g.157502257C>G	GRCh37
NC_000006.10:g.157543949C>G	NCBI36
NG_032093.1:g.408194C>G
NG_032093.2:g.408194C>G
NG_066624.1:g.410098C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3500C>G	ENSP00000055163.8:p.Pro1167Arg
ENST00000414678.8:c.3569C>G	ENSP00000412835.3:p.Pro1190Arg
ENST00000637015.2:c.3788C>G	ENSP00000489729.2:p.Pro1263Arg
ENST00000319584.11:c.1673C>G	ENSP00000313006.7:p.Pro558Arg
ENST00000346085.10:c.3539C>G	ENSP00000344546.5:p.Pro1180Arg
ENST00000350026.10:c.3251C>G	ENSP00000055163.7:p.Pro1084Arg
ENST00000414678.7:c.1817C>G	ENSP00000412835.2:p.Pro606Arg
ENST00000635849.1:c.980C>G	ENSP00000490948.1:p.Pro327Arg
ENST00000635957.1:c.614C>G	ENSP00000490385.1:p.Pro205Arg
ENST00000636930.2:c.3659C>G MANE Select	ENSP00000490491.2:p.Pro1220Arg
ENST00000636940.1:n.1656C>G
ENST00000637015.1:c.1027C>G
ENST00000637568.1:c.941C>G
ENST00000637741.1:n.325C>G
ENST00000637810.1:c.1001C>G	ENSP00000489636.1:p.Pro334Arg
ENST00000637904.1:c.1160C>G	ENSP00000490550.1:p.Pro387Arg
ENST00000647938.1:c.3290C>G	ENSP00000498155.1:p.Pro1097Arg
ENST00000319584.10:c.1676C>G	ENSP00000313006.6:p.Pro559Arg
ENST00000346085.9:c.3290C>G	ENSP00000344546.4:p.Pro1097Arg
ENST00000350026.9:c.3251C>G	ENSP00000055163.7:p.Pro1084Arg
ENST00000400790.3:c.452C>G	ENSP00000383596.3:p.Pro151Arg
ENST00000414678.6:c.1817C>G	ENSP00000412835.2:p.Pro606Arg
ENST00000478761.3:c.861C>G
NM_017519.2:c.3251C>G	NP_059989.2:p.Pro1084Arg
NM_020732.3:c.3290C>G	NP_065783.3:p.Pro1097Arg
XM_005267069.3:c.3410C>G	XP_005267126.2:p.Pro1137Arg
XM_011535984.1:c.2489C>G	XP_011534286.1:p.Pro830Arg
XM_011535985.1:c.2309C>G	XP_011534287.1:p.Pro770Arg
XM_011535986.1:c.2069C>G	XP_011534288.1:p.Pro690Arg
XM_011535987.1:c.1688C>G	XP_011534289.1:p.Pro563Arg
XM_011535988.1:c.551C>G	XP_011534290.1:p.Pro184Arg
NM_001346813.1:c.3410C>G	NP_001333742.1:p.Pro1137Arg
NM_001363725.1:c.1160C>G	NP_001350654.1:p.Pro387Arg
XM_011535984.2:c.3620C>G	XP_011534286.2:p.Pro1207Arg
XM_011535988.3:c.551C>G	XP_011534290.1:p.Pro184Arg
XM_017011103.2:c.3521C>G	XP_016866592.1:p.Pro1174Arg
XM_017011104.1:c.3491C>G	XP_016866593.1:p.Pro1164Arg
XM_017011105.2:c.3461C>G	XP_016866594.1:p.Pro1154Arg
XM_017011106.2:c.3332C>G	XP_016866595.1:p.Pro1111Arg
XM_017011107.2:c.3311C>G	XP_016866596.1:p.Pro1104Arg
XR_002956289.1:n.3703C>G
NM_001363725.2:c.1160C>G	NP_001350654.1:p.Pro387Arg
NM_001371656.1:c.3539C>G	NP_001358585.1:p.Pro1180Arg
NM_001374820.1:c.3539C>G	NP_001361749.1:p.Pro1180Arg
NM_001374828.1:c.3659C>G MANE Select	NP_001361757.1:p.Pro1220Arg
NM_017519.3:c.3500C>G	NP_059989.3:p.Pro1167Arg