Canonical Allele Identifier: CA452990101
Gene: ARID1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.157470041A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148907A>G , CM000668.2:g.157148907A>G GRCh38
NC_000006.11:g.157470041A>G , CM000668.1:g.157470041A>G GRCh37
NC_000006.10:g.157511733A>G NCBI36
NG_032093.1:g.375978A>G
NG_032093.2:g.375978A>G
NG_066624.1:g.377882A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3045A>G ENSP00000055163.8:p.Ala1015=
ENST00000414678.8:c.2955A>G ENSP00000412835.3:p.Ala985=
ENST00000637015.2:c.3045A>G ENSP00000489729.2:p.Ala1015=
ENST00000319584.11:c.1059A>G ENSP00000313006.7:p.Ala353=
ENST00000346085.10:c.3084A>G ENSP00000344546.5:p.Ala1028=
ENST00000350026.10:c.2796A>G ENSP00000055163.7:p.Ala932=
ENST00000414678.7:c.1203A>G ENSP00000412835.2:p.Ala401=
ENST00000452544.2:n.946A>G
ENST00000635849.1:c.366A>G ENSP00000490948.1:p.Ala122=
ENST00000636426.1:n.179A>G
ENST00000636930.2:c.3045A>G MANE Select ENSP00000490491.2:p.Ala1015=
ENST00000637015.1:c.284A>G
ENST00000637568.1:c.88A>G
ENST00000637810.1:c.546A>G ENSP00000489636.1:p.Ala182=
ENST00000637904.1:c.546A>G ENSP00000490550.1:p.Ala182=
ENST00000647938.1:c.2835A>G ENSP00000498155.1:p.Ala945=
ENST00000674190.1:n.1794A>G
ENST00000319584.10:c.1062A>G ENSP00000313006.6:p.Ala354=
ENST00000346085.9:c.2835A>G ENSP00000344546.4:p.Ala945=
ENST00000350026.9:c.2796A>G ENSP00000055163.7:p.Ala932=
ENST00000414678.6:c.1203A>G ENSP00000412835.2:p.Ala401=
ENST00000452544.1:n.892A>G
ENST00000478761.3:c.118A>G
NM_017519.2:c.2796A>G NP_059989.2:p.Ala932=
NM_020732.3:c.2835A>G NP_065783.3:p.Ala945=
XM_005267069.3:c.2796A>G XP_005267126.2:p.Ala932=
XM_011535984.1:c.1746A>G XP_011534286.1:p.Ala582=
XM_011535985.1:c.1566A>G XP_011534287.1:p.Ala522=
XM_011535986.1:c.1326A>G XP_011534288.1:p.Ala442=
XM_011535987.1:c.945A>G XP_011534289.1:p.Ala315=
XM_011535988.1:c.-20+15700A>G XP_011534290.1:n.-20+15700A>G
NM_001346813.1:c.2796A>G NP_001333742.1:p.Ala932=
NM_001363725.1:c.546A>G NP_001350654.1:p.Ala182=
XM_011535984.2:c.2877A>G XP_011534286.2:p.Ala959=
XM_011535988.3:c.-20+15700A>G XP_011534290.1:n.-20+15700A>G
XM_017011103.2:c.2877A>G XP_016866592.1:p.Ala959=
XM_017011104.1:c.2877A>G XP_016866593.1:p.Ala959=
XM_017011105.2:c.2877A>G XP_016866594.1:p.Ala959=
XM_017011106.2:c.2877A>G XP_016866595.1:p.Ala959=
XM_017011107.2:c.2697A>G XP_016866596.1:p.Ala899=
XR_002956289.1:n.2960A>G
NM_001363725.2:c.546A>G NP_001350654.1:p.Ala182=
NM_001371656.1:c.3084A>G NP_001358585.1:p.Ala1028=
NM_001374820.1:c.3084A>G NP_001361749.1:p.Ala1028=
NM_001374828.1:c.3045A>G MANE Select NP_001361757.1:p.Ala1015=
NM_017519.3:c.3045A>G NP_059989.3:p.Ala1015=