Canonical Allele Identifier: CA366389223

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634935
• gnomAD v4: 6-157148909-C-G
• MyVariant Identifiers: chr6:g.157470043C>G (hg19) ; chr6:g.157148909C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148909C>G , CM000668.2:g.157148909C>G	GRCh38
NC_000006.11:g.157470043C>G , CM000668.1:g.157470043C>G	GRCh37
NC_000006.10:g.157511735C>G	NCBI36
NG_032093.1:g.375980C>G
NG_032093.2:g.375980C>G
NG_066624.1:g.377884C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3047C>G	ENSP00000055163.8:p.Ala1016Gly
ENST00000414678.8:c.2957C>G	ENSP00000412835.3:p.Ala986Gly
ENST00000637015.2:c.3047C>G	ENSP00000489729.2:p.Ala1016Gly
ENST00000319584.11:c.1061C>G	ENSP00000313006.7:p.Ala354Gly
ENST00000346085.10:c.3086C>G	ENSP00000344546.5:p.Ala1029Gly
ENST00000350026.10:c.2798C>G	ENSP00000055163.7:p.Ala933Gly
ENST00000414678.7:c.1205C>G	ENSP00000412835.2:p.Ala402Gly
ENST00000452544.2:n.948C>G
ENST00000635849.1:c.368C>G	ENSP00000490948.1:p.Ala123Gly
ENST00000635957.1:c.2C>G	ENSP00000490385.1:p.Ala1Gly
ENST00000636426.1:n.181C>G
ENST00000636930.2:c.3047C>G MANE Select	ENSP00000490491.2:p.Ala1016Gly
ENST00000637015.1:c.286C>G
ENST00000637568.1:c.90C>G
ENST00000637810.1:c.548C>G	ENSP00000489636.1:p.Ala183Gly
ENST00000637904.1:c.548C>G	ENSP00000490550.1:p.Ala183Gly
ENST00000647938.1:c.2837C>G	ENSP00000498155.1:p.Ala946Gly
ENST00000674190.1:n.1796C>G
ENST00000319584.10:c.1064C>G	ENSP00000313006.6:p.Ala355Gly
ENST00000346085.9:c.2837C>G	ENSP00000344546.4:p.Ala946Gly
ENST00000350026.9:c.2798C>G	ENSP00000055163.7:p.Ala933Gly
ENST00000414678.6:c.1205C>G	ENSP00000412835.2:p.Ala402Gly
ENST00000452544.1:n.894C>G
ENST00000478761.3:c.120C>G
NM_017519.2:c.2798C>G	NP_059989.2:p.Ala933Gly
NM_020732.3:c.2837C>G	NP_065783.3:p.Ala946Gly
XM_005267069.3:c.2798C>G	XP_005267126.2:p.Ala933Gly
XM_011535984.1:c.1748C>G	XP_011534286.1:p.Ala583Gly
XM_011535985.1:c.1568C>G	XP_011534287.1:p.Ala523Gly
XM_011535986.1:c.1328C>G	XP_011534288.1:p.Ala443Gly
XM_011535987.1:c.947C>G	XP_011534289.1:p.Ala316Gly
XM_011535988.1:c.-20+15702C>G	XP_011534290.1:n.-20+15702C>G
NM_001346813.1:c.2798C>G	NP_001333742.1:p.Ala933Gly
NM_001363725.1:c.548C>G	NP_001350654.1:p.Ala183Gly
XM_011535984.2:c.2879C>G	XP_011534286.2:p.Ala960Gly
XM_011535988.3:c.-20+15702C>G	XP_011534290.1:n.-20+15702C>G
XM_017011103.2:c.2879C>G	XP_016866592.1:p.Ala960Gly
XM_017011104.1:c.2879C>G	XP_016866593.1:p.Ala960Gly
XM_017011105.2:c.2879C>G	XP_016866594.1:p.Ala960Gly
XM_017011106.2:c.2879C>G	XP_016866595.1:p.Ala960Gly
XM_017011107.2:c.2699C>G	XP_016866596.1:p.Ala900Gly
XR_002956289.1:n.2962C>G
NM_001363725.2:c.548C>G	NP_001350654.1:p.Ala183Gly
NM_001371656.1:c.3086C>G	NP_001358585.1:p.Ala1029Gly
NM_001374820.1:c.3086C>G	NP_001361749.1:p.Ala1029Gly
NM_001374828.1:c.3047C>G MANE Select	NP_001361757.1:p.Ala1016Gly
NM_017519.3:c.3047C>G	NP_059989.3:p.Ala1016Gly