Canonical Allele Identifier: CA366388892
Gene: ARID1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148756C>T , CM000668.2:g.157148756C>T GRCh38
NC_000006.11:g.157469890C>T , CM000668.1:g.157469890C>T GRCh37
NC_000006.10:g.157511582C>T NCBI36
NG_032093.1:g.375827C>T
NG_032093.2:g.375827C>T
NG_066624.1:g.377731C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2894C>T ENSP00000055163.8:p.Pro965Leu
ENST00000414678.8:c.2804C>T ENSP00000412835.3:p.Pro935Leu
ENST00000637015.2:c.2894C>T ENSP00000489729.2:p.Pro965Leu
ENST00000319584.11:c.908C>T ENSP00000313006.7:p.Pro303Leu
ENST00000346085.10:c.2933C>T ENSP00000344546.5:p.Pro978Leu
ENST00000350026.10:c.2645C>T ENSP00000055163.7:p.Pro882Leu
ENST00000414678.7:c.1052C>T ENSP00000412835.2:p.Pro351Leu
ENST00000452544.2:n.795C>T
ENST00000635849.1:c.215C>T ENSP00000490948.1:p.Pro72Leu
ENST00000636426.1:n.28C>T
ENST00000636930.2:c.2894C>T MANE Select ENSP00000490491.2:p.Pro965Leu
ENST00000637015.1:c.133C>T
ENST00000637810.1:c.395C>T ENSP00000489636.1:p.Pro132Leu
ENST00000637904.1:c.395C>T ENSP00000490550.1:p.Pro132Leu
ENST00000647938.1:c.2684C>T ENSP00000498155.1:p.Pro895Leu
ENST00000674190.1:n.1643C>T
ENST00000319584.10:c.911C>T ENSP00000313006.6:p.Pro304Leu
ENST00000346085.9:c.2684C>T ENSP00000344546.4:p.Pro895Leu
ENST00000350026.9:c.2645C>T ENSP00000055163.7:p.Pro882Leu
ENST00000414678.6:c.1052C>T ENSP00000412835.2:p.Pro351Leu
ENST00000452544.1:n.741C>T
NM_017519.2:c.2645C>T NP_059989.2:p.Pro882Leu
NM_020732.3:c.2684C>T NP_065783.3:p.Pro895Leu
XM_005267069.3:c.2645C>T XP_005267126.2:p.Pro882Leu
XM_011535984.1:c.1595C>T XP_011534286.1:p.Pro532Leu
XM_011535985.1:c.1415C>T XP_011534287.1:p.Pro472Leu
XM_011535986.1:c.1175C>T XP_011534288.1:p.Pro392Leu
XM_011535987.1:c.794C>T XP_011534289.1:p.Pro265Leu
XM_011535988.1:c.-20+15549C>T XP_011534290.1:n.-20+15549C>T
NM_001346813.1:c.2645C>T NP_001333742.1:p.Pro882Leu
NM_001363725.1:c.395C>T NP_001350654.1:p.Pro132Leu
XM_011535984.2:c.2726C>T XP_011534286.2:p.Pro909Leu
XM_011535988.3:c.-20+15549C>T XP_011534290.1:n.-20+15549C>T
XM_017011103.2:c.2726C>T XP_016866592.1:p.Pro909Leu
XM_017011104.1:c.2726C>T XP_016866593.1:p.Pro909Leu
XM_017011105.2:c.2726C>T XP_016866594.1:p.Pro909Leu
XM_017011106.2:c.2726C>T XP_016866595.1:p.Pro909Leu
XM_017011107.2:c.2546C>T XP_016866596.1:p.Pro849Leu
XR_002956289.1:n.2809C>T
NM_001363725.2:c.395C>T NP_001350654.1:p.Pro132Leu
NM_001371656.1:c.2933C>T NP_001358585.1:p.Pro978Leu
NM_001374820.1:c.2933C>T NP_001361749.1:p.Pro978Leu
NM_001374828.1:c.2894C>T MANE Select NP_001361757.1:p.Pro965Leu
NM_017519.3:c.2894C>T NP_059989.3:p.Pro965Leu