Canonical Allele Identifier: CA366242424

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522428T>G (hg19) ; chr6:g.157201294T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201294T>G , CM000668.2:g.157201294T>G	GRCh38
NC_000006.11:g.157522428T>G , CM000668.1:g.157522428T>G	GRCh37
NC_000006.10:g.157564120T>G	NCBI36
NG_032093.1:g.428365T>G
NG_032093.2:g.428365T>G
NG_066624.1:g.430269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4910T>G	ENSP00000055163.8:p.Met1637Arg
ENST00000414678.8:c.4979T>G	ENSP00000412835.3:p.Met1660Arg
ENST00000637015.2:c.5198T>G	ENSP00000489729.2:p.Met1733Arg
ENST00000346085.10:c.4949T>G	ENSP00000344546.5:p.Met1650Arg
ENST00000350026.10:c.4661T>G	ENSP00000055163.7:p.Met1554Arg
ENST00000414678.7:c.3227T>G	ENSP00000412835.2:p.Met1076Arg
ENST00000635849.1:c.2390T>G	ENSP00000490948.1:p.Met797Arg
ENST00000635957.1:c.2021T>G	ENSP00000490385.1:p.Met674Arg
ENST00000636227.1:n.3532T>G
ENST00000636254.1:n.989T>G
ENST00000636930.2:c.5069T>G MANE Select	ENSP00000490491.2:p.Met1690Arg
ENST00000636940.1:n.3066T>G
ENST00000637015.1:c.2437T>G
ENST00000637568.1:c.2351T>G
ENST00000637741.1:n.1735T>G
ENST00000637810.1:c.2411T>G	ENSP00000489636.1:p.Met804Arg
ENST00000637904.1:c.2570T>G	ENSP00000490550.1:p.Met857Arg
ENST00000647938.1:c.4700T>G	ENSP00000498155.1:p.Met1567Arg
ENST00000346085.9:c.4700T>G	ENSP00000344546.4:p.Met1567Arg
ENST00000350026.9:c.4661T>G	ENSP00000055163.7:p.Met1554Arg
ENST00000414678.6:c.3227T>G	ENSP00000412835.2:p.Met1076Arg
NM_017519.2:c.4661T>G	NP_059989.2:p.Met1554Arg
NM_020732.3:c.4700T>G	NP_065783.3:p.Met1567Arg
XM_005267069.3:c.4820T>G	XP_005267126.2:p.Met1607Arg
XM_011535984.1:c.3899T>G	XP_011534286.1:p.Met1300Arg
XM_011535985.1:c.3719T>G	XP_011534287.1:p.Met1240Arg
XM_011535986.1:c.3479T>G	XP_011534288.1:p.Met1160Arg
XM_011535987.1:c.3098T>G	XP_011534289.1:p.Met1033Arg
XM_011535988.1:c.1961T>G	XP_011534290.1:p.Met654Arg
NM_001346813.1:c.4820T>G	NP_001333742.1:p.Met1607Arg
NM_001363725.1:c.2570T>G	NP_001350654.1:p.Met857Arg
XM_011535984.2:c.5030T>G	XP_011534286.2:p.Met1677Arg
XM_011535988.3:c.1961T>G	XP_011534290.1:p.Met654Arg
XM_017011103.2:c.4931T>G	XP_016866592.1:p.Met1644Arg
XM_017011104.1:c.4901T>G	XP_016866593.1:p.Met1634Arg
XM_017011105.2:c.4871T>G	XP_016866594.1:p.Met1624Arg
XM_017011106.2:c.4742T>G	XP_016866595.1:p.Met1581Arg
XM_017011107.2:c.4721T>G	XP_016866596.1:p.Met1574Arg
XR_002956289.1:n.5016T>G
NM_001363725.2:c.2570T>G	NP_001350654.1:p.Met857Arg
NM_001371656.1:c.4949T>G	NP_001358585.1:p.Met1650Arg
NM_001374820.1:c.4949T>G	NP_001361749.1:p.Met1650Arg
NM_001374828.1:c.5069T>G MANE Select	NP_001361757.1:p.Met1690Arg
NM_017519.3:c.4910T>G	NP_059989.3:p.Met1637Arg