Canonical Allele Identifier: CA366241102

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521998C>G (hg19) ; chr6:g.157200864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200864C>G , CM000668.2:g.157200864C>G	GRCh38
NC_000006.11:g.157521998C>G , CM000668.1:g.157521998C>G	GRCh37
NC_000006.10:g.157563690C>G	NCBI36
NG_032093.1:g.427935C>G
NG_032093.2:g.427935C>G
NG_066624.1:g.429839C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4480C>G	ENSP00000055163.8:p.Pro1494Ala
ENST00000414678.8:c.4549C>G	ENSP00000412835.3:p.Pro1517Ala
ENST00000637015.2:c.4768C>G	ENSP00000489729.2:p.Pro1590Ala
ENST00000346085.10:c.4519C>G	ENSP00000344546.5:p.Pro1507Ala
ENST00000350026.10:c.4231C>G	ENSP00000055163.7:p.Pro1411Ala
ENST00000414678.7:c.2797C>G	ENSP00000412835.2:p.Pro933Ala
ENST00000635849.1:c.1960C>G	ENSP00000490948.1:p.Pro654Ala
ENST00000635957.1:c.1591C>G	ENSP00000490385.1:p.Pro531Ala
ENST00000636227.1:n.3102C>G
ENST00000636254.1:n.559C>G
ENST00000636930.2:c.4639C>G MANE Select	ENSP00000490491.2:p.Pro1547Ala
ENST00000636940.1:n.2636C>G
ENST00000637015.1:c.2007C>G
ENST00000637568.1:c.1921C>G
ENST00000637741.1:n.1305C>G
ENST00000637810.1:c.1981C>G	ENSP00000489636.1:p.Pro661Ala
ENST00000637904.1:c.2140C>G	ENSP00000490550.1:p.Pro714Ala
ENST00000647938.1:c.4270C>G	ENSP00000498155.1:p.Pro1424Ala
ENST00000346085.9:c.4270C>G	ENSP00000344546.4:p.Pro1424Ala
ENST00000350026.9:c.4231C>G	ENSP00000055163.7:p.Pro1411Ala
ENST00000414678.6:c.2797C>G	ENSP00000412835.2:p.Pro933Ala
NM_017519.2:c.4231C>G	NP_059989.2:p.Pro1411Ala
NM_020732.3:c.4270C>G	NP_065783.3:p.Pro1424Ala
XM_005267069.3:c.4390C>G	XP_005267126.2:p.Pro1464Ala
XM_011535984.1:c.3469C>G	XP_011534286.1:p.Pro1157Ala
XM_011535985.1:c.3289C>G	XP_011534287.1:p.Pro1097Ala
XM_011535986.1:c.3049C>G	XP_011534288.1:p.Pro1017Ala
XM_011535987.1:c.2668C>G	XP_011534289.1:p.Pro890Ala
XM_011535988.1:c.1531C>G	XP_011534290.1:p.Pro511Ala
NM_001346813.1:c.4390C>G	NP_001333742.1:p.Pro1464Ala
NM_001363725.1:c.2140C>G	NP_001350654.1:p.Pro714Ala
XM_011535984.2:c.4600C>G	XP_011534286.2:p.Pro1534Ala
XM_011535988.3:c.1531C>G	XP_011534290.1:p.Pro511Ala
XM_017011103.2:c.4501C>G	XP_016866592.1:p.Pro1501Ala
XM_017011104.1:c.4471C>G	XP_016866593.1:p.Pro1491Ala
XM_017011105.2:c.4441C>G	XP_016866594.1:p.Pro1481Ala
XM_017011106.2:c.4312C>G	XP_016866595.1:p.Pro1438Ala
XM_017011107.2:c.4291C>G	XP_016866596.1:p.Pro1431Ala
XR_002956289.1:n.4586C>G
NM_001363725.2:c.2140C>G	NP_001350654.1:p.Pro714Ala
NM_001371656.1:c.4519C>G	NP_001358585.1:p.Pro1507Ala
NM_001374820.1:c.4519C>G	NP_001361749.1:p.Pro1507Ala
NM_001374828.1:c.4639C>G MANE Select	NP_001361757.1:p.Pro1547Ala
NM_017519.3:c.4480C>G	NP_059989.3:p.Pro1494Ala