Canonical Allele Identifier: CA366242422

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4910T>A	ENSP00000055163.8:p.Met1637Lys
ENST00000414678.8:c.4979T>A	ENSP00000412835.3:p.Met1660Lys
ENST00000637015.2:c.5198T>A	ENSP00000489729.2:p.Met1733Lys
ENST00000346085.10:c.4949T>A	ENSP00000344546.5:p.Met1650Lys
ENST00000350026.10:c.4661T>A	ENSP00000055163.7:p.Met1554Lys
ENST00000414678.7:c.3227T>A	ENSP00000412835.2:p.Met1076Lys
ENST00000635849.1:c.2390T>A	ENSP00000490948.1:p.Met797Lys
ENST00000635957.1:c.2021T>A	ENSP00000490385.1:p.Met674Lys
ENST00000636227.1:n.3532T>A
ENST00000636254.1:n.989T>A
ENST00000636930.2:c.5069T>A MANE Select	ENSP00000490491.2:p.Met1690Lys
ENST00000636940.1:n.3066T>A
ENST00000637015.1:c.2437T>A
ENST00000637568.1:c.2351T>A
ENST00000637741.1:n.1735T>A
ENST00000637810.1:c.2411T>A	ENSP00000489636.1:p.Met804Lys
ENST00000637904.1:c.2570T>A	ENSP00000490550.1:p.Met857Lys
ENST00000647938.1:c.4700T>A	ENSP00000498155.1:p.Met1567Lys
ENST00000346085.9:c.4700T>A	ENSP00000344546.4:p.Met1567Lys
ENST00000350026.9:c.4661T>A	ENSP00000055163.7:p.Met1554Lys
ENST00000414678.6:c.3227T>A	ENSP00000412835.2:p.Met1076Lys
NM_017519.2:c.4661T>A	NP_059989.2:p.Met1554Lys
NM_020732.3:c.4700T>A	NP_065783.3:p.Met1567Lys
XM_005267069.3:c.4820T>A	XP_005267126.2:p.Met1607Lys
XM_011535984.1:c.3899T>A	XP_011534286.1:p.Met1300Lys
XM_011535985.1:c.3719T>A	XP_011534287.1:p.Met1240Lys
XM_011535986.1:c.3479T>A	XP_011534288.1:p.Met1160Lys
XM_011535987.1:c.3098T>A	XP_011534289.1:p.Met1033Lys
XM_011535988.1:c.1961T>A	XP_011534290.1:p.Met654Lys
NM_001346813.1:c.4820T>A	NP_001333742.1:p.Met1607Lys
NM_001363725.1:c.2570T>A	NP_001350654.1:p.Met857Lys
XM_011535984.2:c.5030T>A	XP_011534286.2:p.Met1677Lys
XM_011535988.3:c.1961T>A	XP_011534290.1:p.Met654Lys
XM_017011103.2:c.4931T>A	XP_016866592.1:p.Met1644Lys
XM_017011104.1:c.4901T>A	XP_016866593.1:p.Met1634Lys
XM_017011105.2:c.4871T>A	XP_016866594.1:p.Met1624Lys
XM_017011106.2:c.4742T>A	XP_016866595.1:p.Met1581Lys
XM_017011107.2:c.4721T>A	XP_016866596.1:p.Met1574Lys
XR_002956289.1:n.5016T>A
NM_001363725.2:c.2570T>A	NP_001350654.1:p.Met857Lys
NM_001371656.1:c.4949T>A	NP_001358585.1:p.Met1650Lys
NM_001374820.1:c.4949T>A	NP_001361749.1:p.Met1650Lys
NM_001374828.1:c.5069T>A MANE Select	NP_001361757.1:p.Met1690Lys
NM_017519.3:c.4910T>A	NP_059989.3:p.Met1637Lys