Canonical Allele Identifier: CA366242750

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376248
• MyVariant Identifiers: chr6:g.157522497C>A (hg19) ; chr6:g.157201363C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201363C>A , CM000668.2:g.157201363C>A	GRCh38
NC_000006.11:g.157522497C>A , CM000668.1:g.157522497C>A	GRCh37
NC_000006.10:g.157564189C>A	NCBI36
NG_032093.1:g.428434C>A
NG_032093.2:g.428434C>A
NG_066624.1:g.430338C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4979C>A	ENSP00000055163.8:p.Ser1660Tyr
ENST00000414678.8:c.5048C>A	ENSP00000412835.3:p.Ser1683Tyr
ENST00000637015.2:c.5267C>A	ENSP00000489729.2:p.Ser1756Tyr
ENST00000346085.10:c.5018C>A	ENSP00000344546.5:p.Ser1673Tyr
ENST00000350026.10:c.4730C>A	ENSP00000055163.7:p.Ser1577Tyr
ENST00000414678.7:c.3296C>A	ENSP00000412835.2:p.Ser1099Tyr
ENST00000635849.1:c.2459C>A	ENSP00000490948.1:p.Ser820Tyr
ENST00000635957.1:c.2090C>A	ENSP00000490385.1:p.Ser697Tyr
ENST00000636227.1:n.3601C>A
ENST00000636254.1:n.1058C>A
ENST00000636930.2:c.5138C>A MANE Select	ENSP00000490491.2:p.Ser1713Tyr
ENST00000636940.1:n.3135C>A
ENST00000637015.1:c.2506C>A
ENST00000637568.1:c.2420C>A
ENST00000637741.1:n.1804C>A
ENST00000637810.1:c.2480C>A	ENSP00000489636.1:p.Ser827Tyr
ENST00000637904.1:c.2639C>A	ENSP00000490550.1:p.Ser880Tyr
ENST00000647938.1:c.4769C>A	ENSP00000498155.1:p.Ser1590Tyr
ENST00000346085.9:c.4769C>A	ENSP00000344546.4:p.Ser1590Tyr
ENST00000350026.9:c.4730C>A	ENSP00000055163.7:p.Ser1577Tyr
ENST00000414678.6:c.3296C>A	ENSP00000412835.2:p.Ser1099Tyr
NM_017519.2:c.4730C>A	NP_059989.2:p.Ser1577Tyr
NM_020732.3:c.4769C>A	NP_065783.3:p.Ser1590Tyr
XM_005267069.3:c.4889C>A	XP_005267126.2:p.Ser1630Tyr
XM_011535984.1:c.3968C>A	XP_011534286.1:p.Ser1323Tyr
XM_011535985.1:c.3788C>A	XP_011534287.1:p.Ser1263Tyr
XM_011535986.1:c.3548C>A	XP_011534288.1:p.Ser1183Tyr
XM_011535987.1:c.3167C>A	XP_011534289.1:p.Ser1056Tyr
XM_011535988.1:c.2030C>A	XP_011534290.1:p.Ser677Tyr
NM_001346813.1:c.4889C>A	NP_001333742.1:p.Ser1630Tyr
NM_001363725.1:c.2639C>A	NP_001350654.1:p.Ser880Tyr
XM_011535984.2:c.5099C>A	XP_011534286.2:p.Ser1700Tyr
XM_011535988.3:c.2030C>A	XP_011534290.1:p.Ser677Tyr
XM_017011103.2:c.5000C>A	XP_016866592.1:p.Ser1667Tyr
XM_017011104.1:c.4970C>A	XP_016866593.1:p.Ser1657Tyr
XM_017011105.2:c.4940C>A	XP_016866594.1:p.Ser1647Tyr
XM_017011106.2:c.4811C>A	XP_016866595.1:p.Ser1604Tyr
XM_017011107.2:c.4790C>A	XP_016866596.1:p.Ser1597Tyr
XR_002956289.1:n.5085C>A
NM_001363725.2:c.2639C>A	NP_001350654.1:p.Ser880Tyr
NM_001371656.1:c.5018C>A	NP_001358585.1:p.Ser1673Tyr
NM_001374820.1:c.5018C>A	NP_001361749.1:p.Ser1673Tyr
NM_001374828.1:c.5138C>A MANE Select	NP_001361757.1:p.Ser1713Tyr
NM_017519.3:c.4979C>A	NP_059989.3:p.Ser1660Tyr