Canonical Allele Identifier: CA366388856

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148739-G-T
• MyVariant Identifiers: chr6:g.157469873G>T (hg19) ; chr6:g.157148739G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148739G>T , CM000668.2:g.157148739G>T	GRCh38
NC_000006.11:g.157469873G>T , CM000668.1:g.157469873G>T	GRCh37
NC_000006.10:g.157511565G>T	NCBI36
NG_032093.1:g.375810G>T
NG_032093.2:g.375810G>T
NG_066624.1:g.377714G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2877G>T	ENSP00000055163.8:p.Gln959His
ENST00000414678.8:c.2787G>T	ENSP00000412835.3:p.Gln929His
ENST00000637015.2:c.2877G>T	ENSP00000489729.2:p.Gln959His
ENST00000319584.11:c.891G>T	ENSP00000313006.7:p.Gln297His
ENST00000346085.10:c.2916G>T	ENSP00000344546.5:p.Gln972His
ENST00000350026.10:c.2628G>T	ENSP00000055163.7:p.Gln876His
ENST00000414678.7:c.1035G>T	ENSP00000412835.2:p.Gln345His
ENST00000452544.2:n.778G>T
ENST00000635849.1:c.198G>T	ENSP00000490948.1:p.Gln66His
ENST00000636426.1:n.11G>T
ENST00000636930.2:c.2877G>T MANE Select	ENSP00000490491.2:p.Gln959His
ENST00000637015.1:c.116G>T
ENST00000637810.1:c.378G>T	ENSP00000489636.1:p.Gln126His
ENST00000637904.1:c.378G>T	ENSP00000490550.1:p.Gln126His
ENST00000647938.1:c.2667G>T	ENSP00000498155.1:p.Gln889His
ENST00000674190.1:n.1626G>T
ENST00000319584.10:c.894G>T	ENSP00000313006.6:p.Gln298His
ENST00000346085.9:c.2667G>T	ENSP00000344546.4:p.Gln889His
ENST00000350026.9:c.2628G>T	ENSP00000055163.7:p.Gln876His
ENST00000414678.6:c.1035G>T	ENSP00000412835.2:p.Gln345His
ENST00000452544.1:n.724G>T
NM_017519.2:c.2628G>T	NP_059989.2:p.Gln876His
NM_020732.3:c.2667G>T	NP_065783.3:p.Gln889His
XM_005267069.3:c.2628G>T	XP_005267126.2:p.Gln876His
XM_011535984.1:c.1578G>T	XP_011534286.1:p.Gln526His
XM_011535985.1:c.1398G>T	XP_011534287.1:p.Gln466His
XM_011535986.1:c.1158G>T	XP_011534288.1:p.Gln386His
XM_011535987.1:c.777G>T	XP_011534289.1:p.Gln259His
XM_011535988.1:c.-20+15532G>T	XP_011534290.1:n.-20+15532G>T
NM_001346813.1:c.2628G>T	NP_001333742.1:p.Gln876His
NM_001363725.1:c.378G>T	NP_001350654.1:p.Gln126His
XM_011535984.2:c.2709G>T	XP_011534286.2:p.Gln903His
XM_011535988.3:c.-20+15532G>T	XP_011534290.1:n.-20+15532G>T
XM_017011103.2:c.2709G>T	XP_016866592.1:p.Gln903His
XM_017011104.1:c.2709G>T	XP_016866593.1:p.Gln903His
XM_017011105.2:c.2709G>T	XP_016866594.1:p.Gln903His
XM_017011106.2:c.2709G>T	XP_016866595.1:p.Gln903His
XM_017011107.2:c.2529G>T	XP_016866596.1:p.Gln843His
XR_002956289.1:n.2792G>T
NM_001363725.2:c.378G>T	NP_001350654.1:p.Gln126His
NM_001371656.1:c.2916G>T	NP_001358585.1:p.Gln972His
NM_001374820.1:c.2916G>T	NP_001361749.1:p.Gln972His
NM_001374828.1:c.2877G>T MANE Select	NP_001361757.1:p.Gln959His
NM_017519.3:c.2877G>T	NP_059989.3:p.Gln959His