Canonical Allele Identifier: CA4067170

Gene: ARID1B

Linked Data

• dbSNP Id: rs764978487
• ExAC: 6:157469957 C / T
• gnomAD v2: 6-157469957-C-T
• gnomAD v4: 6-157148823-C-T
• MyVariant Identifiers: chr6:g.157469957C>T (hg19) ; chr6:g.157148823C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148823C>T , CM000668.2:g.157148823C>T	GRCh38
NC_000006.11:g.157469957C>T , CM000668.1:g.157469957C>T	GRCh37
NC_000006.10:g.157511649C>T	NCBI36
NG_032093.1:g.375894C>T
NG_032093.2:g.375894C>T
NG_066624.1:g.377798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2961C>T	ENSP00000055163.8:p.Thr987=
ENST00000414678.8:c.2871C>T	ENSP00000412835.3:p.Thr957=
ENST00000637015.2:c.2961C>T	ENSP00000489729.2:p.Thr987=
ENST00000319584.11:c.975C>T	ENSP00000313006.7:p.Thr325=
ENST00000346085.10:c.3000C>T	ENSP00000344546.5:p.Thr1000=
ENST00000350026.10:c.2712C>T	ENSP00000055163.7:p.Thr904=
ENST00000414678.7:c.1119C>T	ENSP00000412835.2:p.Thr373=
ENST00000452544.2:n.862C>T
ENST00000635849.1:c.282C>T	ENSP00000490948.1:p.Thr94=
ENST00000636426.1:n.95C>T
ENST00000636930.2:c.2961C>T MANE Select	ENSP00000490491.2:p.Thr987=
ENST00000637015.1:c.200C>T
ENST00000637568.1:c.4C>T
ENST00000637810.1:c.462C>T	ENSP00000489636.1:p.Thr154=
ENST00000637904.1:c.462C>T	ENSP00000490550.1:p.Thr154=
ENST00000647938.1:c.2751C>T	ENSP00000498155.1:p.Thr917=
ENST00000674190.1:n.1710C>T
ENST00000319584.10:c.978C>T	ENSP00000313006.6:p.Thr326=
ENST00000346085.9:c.2751C>T	ENSP00000344546.4:p.Thr917=
ENST00000350026.9:c.2712C>T	ENSP00000055163.7:p.Thr904=
ENST00000414678.6:c.1119C>T	ENSP00000412835.2:p.Thr373=
ENST00000452544.1:n.808C>T
ENST00000478761.3:c.34C>T
NM_017519.2:c.2712C>T	NP_059989.2:p.Thr904=
NM_020732.3:c.2751C>T	NP_065783.3:p.Thr917=
XM_005267069.3:c.2712C>T	XP_005267126.2:p.Thr904=
XM_011535984.1:c.1662C>T	XP_011534286.1:p.Thr554=
XM_011535985.1:c.1482C>T	XP_011534287.1:p.Thr494=
XM_011535986.1:c.1242C>T	XP_011534288.1:p.Thr414=
XM_011535987.1:c.861C>T	XP_011534289.1:p.Thr287=
XM_011535988.1:c.-20+15616C>T	XP_011534290.1:n.-20+15616C>T
NM_001346813.1:c.2712C>T	NP_001333742.1:p.Thr904=
NM_001363725.1:c.462C>T	NP_001350654.1:p.Thr154=
XM_011535984.2:c.2793C>T	XP_011534286.2:p.Thr931=
XM_011535988.3:c.-20+15616C>T	XP_011534290.1:n.-20+15616C>T
XM_017011103.2:c.2793C>T	XP_016866592.1:p.Thr931=
XM_017011104.1:c.2793C>T	XP_016866593.1:p.Thr931=
XM_017011105.2:c.2793C>T	XP_016866594.1:p.Thr931=
XM_017011106.2:c.2793C>T	XP_016866595.1:p.Thr931=
XM_017011107.2:c.2613C>T	XP_016866596.1:p.Thr871=
XR_002956289.1:n.2876C>T
NM_001363725.2:c.462C>T	NP_001350654.1:p.Thr154=
NM_001371656.1:c.3000C>T	NP_001358585.1:p.Thr1000=
NM_001374820.1:c.3000C>T	NP_001361749.1:p.Thr1000=
NM_001374828.1:c.2961C>T MANE Select	NP_001361757.1:p.Thr987=
NM_017519.3:c.2961C>T	NP_059989.3:p.Thr987=