Canonical Allele Identifier: CA366242575

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201331-G-T
• MyVariant Identifiers: chr6:g.157522465G>T (hg19) ; chr6:g.157201331G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201331G>T , CM000668.2:g.157201331G>T	GRCh38
NC_000006.11:g.157522465G>T , CM000668.1:g.157522465G>T	GRCh37
NC_000006.10:g.157564157G>T	NCBI36
NG_032093.1:g.428402G>T
NG_032093.2:g.428402G>T
NG_066624.1:g.430306G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4947G>T	ENSP00000055163.8:p.Lys1649Asn
ENST00000414678.8:c.5016G>T	ENSP00000412835.3:p.Lys1672Asn
ENST00000637015.2:c.5235G>T	ENSP00000489729.2:p.Lys1745Asn
ENST00000346085.10:c.4986G>T	ENSP00000344546.5:p.Lys1662Asn
ENST00000350026.10:c.4698G>T	ENSP00000055163.7:p.Lys1566Asn
ENST00000414678.7:c.3264G>T	ENSP00000412835.2:p.Lys1088Asn
ENST00000635849.1:c.2427G>T	ENSP00000490948.1:p.Lys809Asn
ENST00000635957.1:c.2058G>T	ENSP00000490385.1:p.Lys686Asn
ENST00000636227.1:n.3569G>T
ENST00000636254.1:n.1026G>T
ENST00000636930.2:c.5106G>T MANE Select	ENSP00000490491.2:p.Lys1702Asn
ENST00000636940.1:n.3103G>T
ENST00000637015.1:c.2474G>T
ENST00000637568.1:c.2388G>T
ENST00000637741.1:n.1772G>T
ENST00000637810.1:c.2448G>T	ENSP00000489636.1:p.Lys816Asn
ENST00000637904.1:c.2607G>T	ENSP00000490550.1:p.Lys869Asn
ENST00000647938.1:c.4737G>T	ENSP00000498155.1:p.Lys1579Asn
ENST00000346085.9:c.4737G>T	ENSP00000344546.4:p.Lys1579Asn
ENST00000350026.9:c.4698G>T	ENSP00000055163.7:p.Lys1566Asn
ENST00000414678.6:c.3264G>T	ENSP00000412835.2:p.Lys1088Asn
NM_017519.2:c.4698G>T	NP_059989.2:p.Lys1566Asn
NM_020732.3:c.4737G>T	NP_065783.3:p.Lys1579Asn
XM_005267069.3:c.4857G>T	XP_005267126.2:p.Lys1619Asn
XM_011535984.1:c.3936G>T	XP_011534286.1:p.Lys1312Asn
XM_011535985.1:c.3756G>T	XP_011534287.1:p.Lys1252Asn
XM_011535986.1:c.3516G>T	XP_011534288.1:p.Lys1172Asn
XM_011535987.1:c.3135G>T	XP_011534289.1:p.Lys1045Asn
XM_011535988.1:c.1998G>T	XP_011534290.1:p.Lys666Asn
NM_001346813.1:c.4857G>T	NP_001333742.1:p.Lys1619Asn
NM_001363725.1:c.2607G>T	NP_001350654.1:p.Lys869Asn
XM_011535984.2:c.5067G>T	XP_011534286.2:p.Lys1689Asn
XM_011535988.3:c.1998G>T	XP_011534290.1:p.Lys666Asn
XM_017011103.2:c.4968G>T	XP_016866592.1:p.Lys1656Asn
XM_017011104.1:c.4938G>T	XP_016866593.1:p.Lys1646Asn
XM_017011105.2:c.4908G>T	XP_016866594.1:p.Lys1636Asn
XM_017011106.2:c.4779G>T	XP_016866595.1:p.Lys1593Asn
XM_017011107.2:c.4758G>T	XP_016866596.1:p.Lys1586Asn
XR_002956289.1:n.5053G>T
NM_001363725.2:c.2607G>T	NP_001350654.1:p.Lys869Asn
NM_001371656.1:c.4986G>T	NP_001358585.1:p.Lys1662Asn
NM_001374820.1:c.4986G>T	NP_001361749.1:p.Lys1662Asn
NM_001374828.1:c.5106G>T MANE Select	NP_001361757.1:p.Lys1702Asn
NM_017519.3:c.4947G>T	NP_059989.3:p.Lys1649Asn