Canonical Allele Identifier: CA366242423

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4910T>C	ENSP00000055163.8:p.Met1637Thr
ENST00000414678.8:c.4979T>C	ENSP00000412835.3:p.Met1660Thr
ENST00000637015.2:c.5198T>C	ENSP00000489729.2:p.Met1733Thr
ENST00000346085.10:c.4949T>C	ENSP00000344546.5:p.Met1650Thr
ENST00000350026.10:c.4661T>C	ENSP00000055163.7:p.Met1554Thr
ENST00000414678.7:c.3227T>C	ENSP00000412835.2:p.Met1076Thr
ENST00000635849.1:c.2390T>C	ENSP00000490948.1:p.Met797Thr
ENST00000635957.1:c.2021T>C	ENSP00000490385.1:p.Met674Thr
ENST00000636227.1:n.3532T>C
ENST00000636254.1:n.989T>C
ENST00000636930.2:c.5069T>C MANE Select	ENSP00000490491.2:p.Met1690Thr
ENST00000636940.1:n.3066T>C
ENST00000637015.1:c.2437T>C
ENST00000637568.1:c.2351T>C
ENST00000637741.1:n.1735T>C
ENST00000637810.1:c.2411T>C	ENSP00000489636.1:p.Met804Thr
ENST00000637904.1:c.2570T>C	ENSP00000490550.1:p.Met857Thr
ENST00000647938.1:c.4700T>C	ENSP00000498155.1:p.Met1567Thr
ENST00000346085.9:c.4700T>C	ENSP00000344546.4:p.Met1567Thr
ENST00000350026.9:c.4661T>C	ENSP00000055163.7:p.Met1554Thr
ENST00000414678.6:c.3227T>C	ENSP00000412835.2:p.Met1076Thr
NM_017519.2:c.4661T>C	NP_059989.2:p.Met1554Thr
NM_020732.3:c.4700T>C	NP_065783.3:p.Met1567Thr
XM_005267069.3:c.4820T>C	XP_005267126.2:p.Met1607Thr
XM_011535984.1:c.3899T>C	XP_011534286.1:p.Met1300Thr
XM_011535985.1:c.3719T>C	XP_011534287.1:p.Met1240Thr
XM_011535986.1:c.3479T>C	XP_011534288.1:p.Met1160Thr
XM_011535987.1:c.3098T>C	XP_011534289.1:p.Met1033Thr
XM_011535988.1:c.1961T>C	XP_011534290.1:p.Met654Thr
NM_001346813.1:c.4820T>C	NP_001333742.1:p.Met1607Thr
NM_001363725.1:c.2570T>C	NP_001350654.1:p.Met857Thr
XM_011535984.2:c.5030T>C	XP_011534286.2:p.Met1677Thr
XM_011535988.3:c.1961T>C	XP_011534290.1:p.Met654Thr
XM_017011103.2:c.4931T>C	XP_016866592.1:p.Met1644Thr
XM_017011104.1:c.4901T>C	XP_016866593.1:p.Met1634Thr
XM_017011105.2:c.4871T>C	XP_016866594.1:p.Met1624Thr
XM_017011106.2:c.4742T>C	XP_016866595.1:p.Met1581Thr
XM_017011107.2:c.4721T>C	XP_016866596.1:p.Met1574Thr
XR_002956289.1:n.5016T>C
NM_001363725.2:c.2570T>C	NP_001350654.1:p.Met857Thr
NM_001371656.1:c.4949T>C	NP_001358585.1:p.Met1650Thr
NM_001374820.1:c.4949T>C	NP_001361749.1:p.Met1650Thr
NM_001374828.1:c.5069T>C MANE Select	NP_001361757.1:p.Met1690Thr
NM_017519.3:c.4910T>C	NP_059989.3:p.Met1637Thr