Canonical Allele Identifier: CA208181
Community Standard Title: NM_001374828.1(ARID1B):c.6049C>T (p.Pro2017Ser)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206821C>T , CM000668.2:g.157206821C>T GRCh38
NC_000006.11:g.157527955C>T , CM000668.1:g.157527955C>T GRCh37
NC_000006.10:g.157569647C>T NCBI36
NG_032093.1:g.433892C>T
NG_032093.2:g.433892C>T
NG_066624.1:g.435796C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6049C>T MANE Select NP_001361757.1:p.Pro2017Ser
ENST00000636930.2:c.6049C>T MANE Select ENSP00000490491.2:p.Pro2017Ser
NM_001346813.1:c.5800C>T NP_001333742.1:p.Pro1934Ser
NM_001363725.1:c.3550C>T NP_001350654.1:p.Pro1184Ser
NM_001363725.2:c.3550C>T NP_001350654.1:p.Pro1184Ser
NM_001371656.1:c.5929C>T NP_001358585.1:p.Pro1977Ser
NM_001374820.1:c.5929C>T NP_001361749.1:p.Pro1977Ser
NM_017519.2:c.5641C>T NP_059989.2:p.Pro1881Ser
NM_017519.3:c.5890C>T NP_059989.3:p.Pro1964Ser
NM_020732.3:c.5680C>T NP_065783.3:p.Pro1894Ser
ENST00000346085.10:c.5929C>T ENSP00000344546.5:p.Pro1977Ser
ENST00000346085.9:c.5680C>T ENSP00000344546.4:p.Pro1894Ser
ENST00000350026.10:c.5641C>T ENSP00000055163.7:p.Pro1881Ser
ENST00000350026.11:c.5890C>T ENSP00000055163.8:p.Pro1964Ser
ENST00000350026.9:c.5641C>T ENSP00000055163.7:p.Pro1881Ser
ENST00000414678.6:c.4207C>T ENSP00000412835.2:p.Pro1403Ser
ENST00000414678.7:c.4207C>T ENSP00000412835.2:p.Pro1403Ser
ENST00000414678.8:c.5959C>T ENSP00000412835.3:p.Pro1987Ser
ENST00000635849.1:c.3370C>T ENSP00000490948.1:p.Pro1124Ser
ENST00000635928.1:c.205C>T ENSP00000489717.1:p.Pro69Ser
ENST00000635957.1:c.3001C>T ENSP00000490385.1:p.Pro1001Ser
ENST00000636227.1:n.4512C>T
ENST00000636254.1:n.1969C>T
ENST00000636940.1:n.4046C>T
ENST00000637015.1:c.3417C>T
ENST00000637015.2:c.6178C>T ENSP00000489729.2:p.Pro2060Ser
ENST00000637568.1:c.3331C>T
ENST00000637741.1:n.2715C>T
ENST00000637810.1:c.3391C>T ENSP00000489636.1:p.Pro1131Ser
ENST00000637904.1:c.3550C>T ENSP00000490550.1:p.Pro1184Ser
ENST00000637933.1:n.3164C>T
ENST00000647938.1:c.5680C>T ENSP00000498155.1:p.Pro1894Ser
XM_005267069.3:c.5800C>T XP_005267126.2:p.Pro1934Ser
XM_011535984.1:c.4879C>T XP_011534286.1:p.Pro1627Ser
XM_011535984.2:c.6010C>T XP_011534286.2:p.Pro2004Ser
XM_011535985.1:c.4699C>T XP_011534287.1:p.Pro1567Ser
XM_011535986.1:c.4459C>T XP_011534288.1:p.Pro1487Ser
XM_011535987.1:c.4078C>T XP_011534289.1:p.Pro1360Ser
XM_011535988.1:c.2941C>T XP_011534290.1:p.Pro981Ser
XM_011535988.3:c.2941C>T XP_011534290.1:p.Pro981Ser
XM_017011103.2:c.5911C>T XP_016866592.1:p.Pro1971Ser
XM_017011104.1:c.5881C>T XP_016866593.1:p.Pro1961Ser
XM_017011105.2:c.5851C>T XP_016866594.1:p.Pro1951Ser
XM_017011106.2:c.5722C>T XP_016866595.1:p.Pro1908Ser
XM_017011107.2:c.5701C>T XP_016866596.1:p.Pro1901Ser
XR_002956289.1:n.5996C>T