Canonical Allele Identifier: CA366242749

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4979C>T	ENSP00000055163.8:p.Ser1660Phe
ENST00000414678.8:c.5048C>T	ENSP00000412835.3:p.Ser1683Phe
ENST00000637015.2:c.5267C>T	ENSP00000489729.2:p.Ser1756Phe
ENST00000346085.10:c.5018C>T	ENSP00000344546.5:p.Ser1673Phe
ENST00000350026.10:c.4730C>T	ENSP00000055163.7:p.Ser1577Phe
ENST00000414678.7:c.3296C>T	ENSP00000412835.2:p.Ser1099Phe
ENST00000635849.1:c.2459C>T	ENSP00000490948.1:p.Ser820Phe
ENST00000635957.1:c.2090C>T	ENSP00000490385.1:p.Ser697Phe
ENST00000636227.1:n.3601C>T
ENST00000636254.1:n.1058C>T
ENST00000636930.2:c.5138C>T MANE Select	ENSP00000490491.2:p.Ser1713Phe
ENST00000636940.1:n.3135C>T
ENST00000637015.1:c.2506C>T
ENST00000637568.1:c.2420C>T
ENST00000637741.1:n.1804C>T
ENST00000637810.1:c.2480C>T	ENSP00000489636.1:p.Ser827Phe
ENST00000637904.1:c.2639C>T	ENSP00000490550.1:p.Ser880Phe
ENST00000647938.1:c.4769C>T	ENSP00000498155.1:p.Ser1590Phe
ENST00000346085.9:c.4769C>T	ENSP00000344546.4:p.Ser1590Phe
ENST00000350026.9:c.4730C>T	ENSP00000055163.7:p.Ser1577Phe
ENST00000414678.6:c.3296C>T	ENSP00000412835.2:p.Ser1099Phe
NM_017519.2:c.4730C>T	NP_059989.2:p.Ser1577Phe
NM_020732.3:c.4769C>T	NP_065783.3:p.Ser1590Phe
XM_005267069.3:c.4889C>T	XP_005267126.2:p.Ser1630Phe
XM_011535984.1:c.3968C>T	XP_011534286.1:p.Ser1323Phe
XM_011535985.1:c.3788C>T	XP_011534287.1:p.Ser1263Phe
XM_011535986.1:c.3548C>T	XP_011534288.1:p.Ser1183Phe
XM_011535987.1:c.3167C>T	XP_011534289.1:p.Ser1056Phe
XM_011535988.1:c.2030C>T	XP_011534290.1:p.Ser677Phe
NM_001346813.1:c.4889C>T	NP_001333742.1:p.Ser1630Phe
NM_001363725.1:c.2639C>T	NP_001350654.1:p.Ser880Phe
XM_011535984.2:c.5099C>T	XP_011534286.2:p.Ser1700Phe
XM_011535988.3:c.2030C>T	XP_011534290.1:p.Ser677Phe
XM_017011103.2:c.5000C>T	XP_016866592.1:p.Ser1667Phe
XM_017011104.1:c.4970C>T	XP_016866593.1:p.Ser1657Phe
XM_017011105.2:c.4940C>T	XP_016866594.1:p.Ser1647Phe
XM_017011106.2:c.4811C>T	XP_016866595.1:p.Ser1604Phe
XM_017011107.2:c.4790C>T	XP_016866596.1:p.Ser1597Phe
XR_002956289.1:n.5085C>T
NM_001363725.2:c.2639C>T	NP_001350654.1:p.Ser880Phe
NM_001371656.1:c.5018C>T	NP_001358585.1:p.Ser1673Phe
NM_001374820.1:c.5018C>T	NP_001361749.1:p.Ser1673Phe
NM_001374828.1:c.5138C>T MANE Select	NP_001361757.1:p.Ser1713Phe
NM_017519.3:c.4979C>T	NP_059989.3:p.Ser1660Phe