Canonical Allele Identifier: CA366242491

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522449T>C (hg19) ; chr6:g.157201315T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201315T>C , CM000668.2:g.157201315T>C	GRCh38
NC_000006.11:g.157522449T>C , CM000668.1:g.157522449T>C	GRCh37
NC_000006.10:g.157564141T>C	NCBI36
NG_032093.1:g.428386T>C
NG_032093.2:g.428386T>C
NG_066624.1:g.430290T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4931T>C	ENSP00000055163.8:p.Phe1644Ser
ENST00000414678.8:c.5000T>C	ENSP00000412835.3:p.Phe1667Ser
ENST00000637015.2:c.5219T>C	ENSP00000489729.2:p.Phe1740Ser
ENST00000346085.10:c.4970T>C	ENSP00000344546.5:p.Phe1657Ser
ENST00000350026.10:c.4682T>C	ENSP00000055163.7:p.Phe1561Ser
ENST00000414678.7:c.3248T>C	ENSP00000412835.2:p.Phe1083Ser
ENST00000635849.1:c.2411T>C	ENSP00000490948.1:p.Phe804Ser
ENST00000635957.1:c.2042T>C	ENSP00000490385.1:p.Phe681Ser
ENST00000636227.1:n.3553T>C
ENST00000636254.1:n.1010T>C
ENST00000636930.2:c.5090T>C MANE Select	ENSP00000490491.2:p.Phe1697Ser
ENST00000636940.1:n.3087T>C
ENST00000637015.1:c.2458T>C
ENST00000637568.1:c.2372T>C
ENST00000637741.1:n.1756T>C
ENST00000637810.1:c.2432T>C	ENSP00000489636.1:p.Phe811Ser
ENST00000637904.1:c.2591T>C	ENSP00000490550.1:p.Phe864Ser
ENST00000647938.1:c.4721T>C	ENSP00000498155.1:p.Phe1574Ser
ENST00000346085.9:c.4721T>C	ENSP00000344546.4:p.Phe1574Ser
ENST00000350026.9:c.4682T>C	ENSP00000055163.7:p.Phe1561Ser
ENST00000414678.6:c.3248T>C	ENSP00000412835.2:p.Phe1083Ser
NM_017519.2:c.4682T>C	NP_059989.2:p.Phe1561Ser
NM_020732.3:c.4721T>C	NP_065783.3:p.Phe1574Ser
XM_005267069.3:c.4841T>C	XP_005267126.2:p.Phe1614Ser
XM_011535984.1:c.3920T>C	XP_011534286.1:p.Phe1307Ser
XM_011535985.1:c.3740T>C	XP_011534287.1:p.Phe1247Ser
XM_011535986.1:c.3500T>C	XP_011534288.1:p.Phe1167Ser
XM_011535987.1:c.3119T>C	XP_011534289.1:p.Phe1040Ser
XM_011535988.1:c.1982T>C	XP_011534290.1:p.Phe661Ser
NM_001346813.1:c.4841T>C	NP_001333742.1:p.Phe1614Ser
NM_001363725.1:c.2591T>C	NP_001350654.1:p.Phe864Ser
XM_011535984.2:c.5051T>C	XP_011534286.2:p.Phe1684Ser
XM_011535988.3:c.1982T>C	XP_011534290.1:p.Phe661Ser
XM_017011103.2:c.4952T>C	XP_016866592.1:p.Phe1651Ser
XM_017011104.1:c.4922T>C	XP_016866593.1:p.Phe1641Ser
XM_017011105.2:c.4892T>C	XP_016866594.1:p.Phe1631Ser
XM_017011106.2:c.4763T>C	XP_016866595.1:p.Phe1588Ser
XM_017011107.2:c.4742T>C	XP_016866596.1:p.Phe1581Ser
XR_002956289.1:n.5037T>C
NM_001363725.2:c.2591T>C	NP_001350654.1:p.Phe864Ser
NM_001371656.1:c.4970T>C	NP_001358585.1:p.Phe1657Ser
NM_001374820.1:c.4970T>C	NP_001361749.1:p.Phe1657Ser
NM_001374828.1:c.5090T>C MANE Select	NP_001361757.1:p.Phe1697Ser
NM_017519.3:c.4931T>C	NP_059989.3:p.Phe1644Ser