Canonical Allele Identifier: CA366241980

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374558
• MyVariant Identifiers: chr6:g.157522232C>G (hg19) ; chr6:g.157201098C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201098C>G , CM000668.2:g.157201098C>G	GRCh38
NC_000006.11:g.157522232C>G , CM000668.1:g.157522232C>G	GRCh37
NC_000006.10:g.157563924C>G	NCBI36
NG_032093.1:g.428169C>G
NG_032093.2:g.428169C>G
NG_066624.1:g.430073C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4714C>G	ENSP00000055163.8:p.Pro1572Ala
ENST00000414678.8:c.4783C>G	ENSP00000412835.3:p.Pro1595Ala
ENST00000637015.2:c.5002C>G	ENSP00000489729.2:p.Pro1668Ala
ENST00000346085.10:c.4753C>G	ENSP00000344546.5:p.Pro1585Ala
ENST00000350026.10:c.4465C>G	ENSP00000055163.7:p.Pro1489Ala
ENST00000414678.7:c.3031C>G	ENSP00000412835.2:p.Pro1011Ala
ENST00000635849.1:c.2194C>G	ENSP00000490948.1:p.Pro732Ala
ENST00000635957.1:c.1825C>G	ENSP00000490385.1:p.Pro609Ala
ENST00000636227.1:n.3336C>G
ENST00000636254.1:n.793C>G
ENST00000636930.2:c.4873C>G MANE Select	ENSP00000490491.2:p.Pro1625Ala
ENST00000636940.1:n.2870C>G
ENST00000637015.1:c.2241C>G
ENST00000637568.1:c.2155C>G
ENST00000637741.1:n.1539C>G
ENST00000637810.1:c.2215C>G	ENSP00000489636.1:p.Pro739Ala
ENST00000637904.1:c.2374C>G	ENSP00000490550.1:p.Pro792Ala
ENST00000647938.1:c.4504C>G	ENSP00000498155.1:p.Pro1502Ala
ENST00000346085.9:c.4504C>G	ENSP00000344546.4:p.Pro1502Ala
ENST00000350026.9:c.4465C>G	ENSP00000055163.7:p.Pro1489Ala
ENST00000414678.6:c.3031C>G	ENSP00000412835.2:p.Pro1011Ala
NM_017519.2:c.4465C>G	NP_059989.2:p.Pro1489Ala
NM_020732.3:c.4504C>G	NP_065783.3:p.Pro1502Ala
XM_005267069.3:c.4624C>G	XP_005267126.2:p.Pro1542Ala
XM_011535984.1:c.3703C>G	XP_011534286.1:p.Pro1235Ala
XM_011535985.1:c.3523C>G	XP_011534287.1:p.Pro1175Ala
XM_011535986.1:c.3283C>G	XP_011534288.1:p.Pro1095Ala
XM_011535987.1:c.2902C>G	XP_011534289.1:p.Pro968Ala
XM_011535988.1:c.1765C>G	XP_011534290.1:p.Pro589Ala
NM_001346813.1:c.4624C>G	NP_001333742.1:p.Pro1542Ala
NM_001363725.1:c.2374C>G	NP_001350654.1:p.Pro792Ala
XM_011535984.2:c.4834C>G	XP_011534286.2:p.Pro1612Ala
XM_011535988.3:c.1765C>G	XP_011534290.1:p.Pro589Ala
XM_017011103.2:c.4735C>G	XP_016866592.1:p.Pro1579Ala
XM_017011104.1:c.4705C>G	XP_016866593.1:p.Pro1569Ala
XM_017011105.2:c.4675C>G	XP_016866594.1:p.Pro1559Ala
XM_017011106.2:c.4546C>G	XP_016866595.1:p.Pro1516Ala
XM_017011107.2:c.4525C>G	XP_016866596.1:p.Pro1509Ala
XR_002956289.1:n.4820C>G
NM_001363725.2:c.2374C>G	NP_001350654.1:p.Pro792Ala
NM_001371656.1:c.4753C>G	NP_001358585.1:p.Pro1585Ala
NM_001374820.1:c.4753C>G	NP_001361749.1:p.Pro1585Ala
NM_001374828.1:c.4873C>G MANE Select	NP_001361757.1:p.Pro1625Ala
NM_017519.3:c.4714C>G	NP_059989.3:p.Pro1572Ala