Canonical Allele Identifier: CA366242427

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522429G>T (hg19) ; chr6:g.157201295G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201295G>T , CM000668.2:g.157201295G>T	GRCh38
NC_000006.11:g.157522429G>T , CM000668.1:g.157522429G>T	GRCh37
NC_000006.10:g.157564121G>T	NCBI36
NG_032093.1:g.428366G>T
NG_032093.2:g.428366G>T
NG_066624.1:g.430270G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4911G>T	ENSP00000055163.8:p.Met1637Ile
ENST00000414678.8:c.4980G>T	ENSP00000412835.3:p.Met1660Ile
ENST00000637015.2:c.5199G>T	ENSP00000489729.2:p.Met1733Ile
ENST00000346085.10:c.4950G>T	ENSP00000344546.5:p.Met1650Ile
ENST00000350026.10:c.4662G>T	ENSP00000055163.7:p.Met1554Ile
ENST00000414678.7:c.3228G>T	ENSP00000412835.2:p.Met1076Ile
ENST00000635849.1:c.2391G>T	ENSP00000490948.1:p.Met797Ile
ENST00000635957.1:c.2022G>T	ENSP00000490385.1:p.Met674Ile
ENST00000636227.1:n.3533G>T
ENST00000636254.1:n.990G>T
ENST00000636930.2:c.5070G>T MANE Select	ENSP00000490491.2:p.Met1690Ile
ENST00000636940.1:n.3067G>T
ENST00000637015.1:c.2438G>T
ENST00000637568.1:c.2352G>T
ENST00000637741.1:n.1736G>T
ENST00000637810.1:c.2412G>T	ENSP00000489636.1:p.Met804Ile
ENST00000637904.1:c.2571G>T	ENSP00000490550.1:p.Met857Ile
ENST00000647938.1:c.4701G>T	ENSP00000498155.1:p.Met1567Ile
ENST00000346085.9:c.4701G>T	ENSP00000344546.4:p.Met1567Ile
ENST00000350026.9:c.4662G>T	ENSP00000055163.7:p.Met1554Ile
ENST00000414678.6:c.3228G>T	ENSP00000412835.2:p.Met1076Ile
NM_017519.2:c.4662G>T	NP_059989.2:p.Met1554Ile
NM_020732.3:c.4701G>T	NP_065783.3:p.Met1567Ile
XM_005267069.3:c.4821G>T	XP_005267126.2:p.Met1607Ile
XM_011535984.1:c.3900G>T	XP_011534286.1:p.Met1300Ile
XM_011535985.1:c.3720G>T	XP_011534287.1:p.Met1240Ile
XM_011535986.1:c.3480G>T	XP_011534288.1:p.Met1160Ile
XM_011535987.1:c.3099G>T	XP_011534289.1:p.Met1033Ile
XM_011535988.1:c.1962G>T	XP_011534290.1:p.Met654Ile
NM_001346813.1:c.4821G>T	NP_001333742.1:p.Met1607Ile
NM_001363725.1:c.2571G>T	NP_001350654.1:p.Met857Ile
XM_011535984.2:c.5031G>T	XP_011534286.2:p.Met1677Ile
XM_011535988.3:c.1962G>T	XP_011534290.1:p.Met654Ile
XM_017011103.2:c.4932G>T	XP_016866592.1:p.Met1644Ile
XM_017011104.1:c.4902G>T	XP_016866593.1:p.Met1634Ile
XM_017011105.2:c.4872G>T	XP_016866594.1:p.Met1624Ile
XM_017011106.2:c.4743G>T	XP_016866595.1:p.Met1581Ile
XM_017011107.2:c.4722G>T	XP_016866596.1:p.Met1574Ile
XR_002956289.1:n.5017G>T
NM_001363725.2:c.2571G>T	NP_001350654.1:p.Met857Ile
NM_001371656.1:c.4950G>T	NP_001358585.1:p.Met1650Ile
NM_001374820.1:c.4950G>T	NP_001361749.1:p.Met1650Ile
NM_001374828.1:c.5070G>T MANE Select	NP_001361757.1:p.Met1690Ile
NM_017519.3:c.4911G>T	NP_059989.3:p.Met1637Ile