Canonical Allele Identifier: CA366242316

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522376A>T (hg19) ; chr6:g.157201242A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201242A>T , CM000668.2:g.157201242A>T	GRCh38
NC_000006.11:g.157522376A>T , CM000668.1:g.157522376A>T	GRCh37
NC_000006.10:g.157564068A>T	NCBI36
NG_032093.1:g.428313A>T
NG_032093.2:g.428313A>T
NG_066624.1:g.430217A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4858A>T	ENSP00000055163.8:p.Ile1620Phe
ENST00000414678.8:c.4927A>T	ENSP00000412835.3:p.Ile1643Phe
ENST00000637015.2:c.5146A>T	ENSP00000489729.2:p.Ile1716Phe
ENST00000346085.10:c.4897A>T	ENSP00000344546.5:p.Ile1633Phe
ENST00000350026.10:c.4609A>T	ENSP00000055163.7:p.Ile1537Phe
ENST00000414678.7:c.3175A>T	ENSP00000412835.2:p.Ile1059Phe
ENST00000635849.1:c.2338A>T	ENSP00000490948.1:p.Ile780Phe
ENST00000635957.1:c.1969A>T	ENSP00000490385.1:p.Ile657Phe
ENST00000636227.1:n.3480A>T
ENST00000636254.1:n.937A>T
ENST00000636930.2:c.5017A>T MANE Select	ENSP00000490491.2:p.Ile1673Phe
ENST00000636940.1:n.3014A>T
ENST00000637015.1:c.2385A>T
ENST00000637568.1:c.2299A>T
ENST00000637741.1:n.1683A>T
ENST00000637810.1:c.2359A>T	ENSP00000489636.1:p.Ile787Phe
ENST00000637904.1:c.2518A>T	ENSP00000490550.1:p.Ile840Phe
ENST00000647938.1:c.4648A>T	ENSP00000498155.1:p.Ile1550Phe
ENST00000346085.9:c.4648A>T	ENSP00000344546.4:p.Ile1550Phe
ENST00000350026.9:c.4609A>T	ENSP00000055163.7:p.Ile1537Phe
ENST00000414678.6:c.3175A>T	ENSP00000412835.2:p.Ile1059Phe
NM_017519.2:c.4609A>T	NP_059989.2:p.Ile1537Phe
NM_020732.3:c.4648A>T	NP_065783.3:p.Ile1550Phe
XM_005267069.3:c.4768A>T	XP_005267126.2:p.Ile1590Phe
XM_011535984.1:c.3847A>T	XP_011534286.1:p.Ile1283Phe
XM_011535985.1:c.3667A>T	XP_011534287.1:p.Ile1223Phe
XM_011535986.1:c.3427A>T	XP_011534288.1:p.Ile1143Phe
XM_011535987.1:c.3046A>T	XP_011534289.1:p.Ile1016Phe
XM_011535988.1:c.1909A>T	XP_011534290.1:p.Ile637Phe
NM_001346813.1:c.4768A>T	NP_001333742.1:p.Ile1590Phe
NM_001363725.1:c.2518A>T	NP_001350654.1:p.Ile840Phe
XM_011535984.2:c.4978A>T	XP_011534286.2:p.Ile1660Phe
XM_011535988.3:c.1909A>T	XP_011534290.1:p.Ile637Phe
XM_017011103.2:c.4879A>T	XP_016866592.1:p.Ile1627Phe
XM_017011104.1:c.4849A>T	XP_016866593.1:p.Ile1617Phe
XM_017011105.2:c.4819A>T	XP_016866594.1:p.Ile1607Phe
XM_017011106.2:c.4690A>T	XP_016866595.1:p.Ile1564Phe
XM_017011107.2:c.4669A>T	XP_016866596.1:p.Ile1557Phe
XR_002956289.1:n.4964A>T
NM_001363725.2:c.2518A>T	NP_001350654.1:p.Ile840Phe
NM_001371656.1:c.4897A>T	NP_001358585.1:p.Ile1633Phe
NM_001374820.1:c.4897A>T	NP_001361749.1:p.Ile1633Phe
NM_001374828.1:c.5017A>T MANE Select	NP_001361757.1:p.Ile1673Phe
NM_017519.3:c.4858A>T	NP_059989.3:p.Ile1620Phe