Canonical Allele Identifier: CA150370361

Gene: ARID1B

Linked Data

• dbSNP Id: rs966591249
• gnomAD v2: 6-157522378-C-T
• gnomAD v4: 6-157201244-C-T
• MyVariant Identifiers: chr6:g.157522378C>T (hg19) ; chr6:g.157201244C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201244C>T , CM000668.2:g.157201244C>T	GRCh38
NC_000006.11:g.157522378C>T , CM000668.1:g.157522378C>T	GRCh37
NC_000006.10:g.157564070C>T	NCBI36
NG_032093.1:g.428315C>T
NG_032093.2:g.428315C>T
NG_066624.1:g.430219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4860C>T	ENSP00000055163.8:p.Ile1620=
ENST00000414678.8:c.4929C>T	ENSP00000412835.3:p.Ile1643=
ENST00000637015.2:c.5148C>T	ENSP00000489729.2:p.Ile1716=
ENST00000346085.10:c.4899C>T	ENSP00000344546.5:p.Ile1633=
ENST00000350026.10:c.4611C>T	ENSP00000055163.7:p.Ile1537=
ENST00000414678.7:c.3177C>T	ENSP00000412835.2:p.Ile1059=
ENST00000635849.1:c.2340C>T	ENSP00000490948.1:p.Ile780=
ENST00000635957.1:c.1971C>T	ENSP00000490385.1:p.Ile657=
ENST00000636227.1:n.3482C>T
ENST00000636254.1:n.939C>T
ENST00000636930.2:c.5019C>T MANE Select	ENSP00000490491.2:p.Ile1673=
ENST00000636940.1:n.3016C>T
ENST00000637015.1:c.2387C>T
ENST00000637568.1:c.2301C>T
ENST00000637741.1:n.1685C>T
ENST00000637810.1:c.2361C>T	ENSP00000489636.1:p.Ile787=
ENST00000637904.1:c.2520C>T	ENSP00000490550.1:p.Ile840=
ENST00000647938.1:c.4650C>T	ENSP00000498155.1:p.Ile1550=
ENST00000346085.9:c.4650C>T	ENSP00000344546.4:p.Ile1550=
ENST00000350026.9:c.4611C>T	ENSP00000055163.7:p.Ile1537=
ENST00000414678.6:c.3177C>T	ENSP00000412835.2:p.Ile1059=
NM_017519.2:c.4611C>T	NP_059989.2:p.Ile1537=
NM_020732.3:c.4650C>T	NP_065783.3:p.Ile1550=
XM_005267069.3:c.4770C>T	XP_005267126.2:p.Ile1590=
XM_011535984.1:c.3849C>T	XP_011534286.1:p.Ile1283=
XM_011535985.1:c.3669C>T	XP_011534287.1:p.Ile1223=
XM_011535986.1:c.3429C>T	XP_011534288.1:p.Ile1143=
XM_011535987.1:c.3048C>T	XP_011534289.1:p.Ile1016=
XM_011535988.1:c.1911C>T	XP_011534290.1:p.Ile637=
NM_001346813.1:c.4770C>T	NP_001333742.1:p.Ile1590=
NM_001363725.1:c.2520C>T	NP_001350654.1:p.Ile840=
XM_011535984.2:c.4980C>T	XP_011534286.2:p.Ile1660=
XM_011535988.3:c.1911C>T	XP_011534290.1:p.Ile637=
XM_017011103.2:c.4881C>T	XP_016866592.1:p.Ile1627=
XM_017011104.1:c.4851C>T	XP_016866593.1:p.Ile1617=
XM_017011105.2:c.4821C>T	XP_016866594.1:p.Ile1607=
XM_017011106.2:c.4692C>T	XP_016866595.1:p.Ile1564=
XM_017011107.2:c.4671C>T	XP_016866596.1:p.Ile1557=
XR_002956289.1:n.4966C>T
NM_001363725.2:c.2520C>T	NP_001350654.1:p.Ile840=
NM_001371656.1:c.4899C>T	NP_001358585.1:p.Ile1633=
NM_001374820.1:c.4899C>T	NP_001361749.1:p.Ile1633=
NM_001374828.1:c.5019C>T MANE Select	NP_001361757.1:p.Ile1673=
NM_017519.3:c.4860C>T	NP_059989.3:p.Ile1620=