Canonical Allele Identifier: CA4067972
Community Standard Title: NM_001374828.1(ARID1B):c.6218A>G (p.Asn2073Ser)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206990A>G , CM000668.2:g.157206990A>G GRCh38
NC_000006.11:g.157528124A>G , CM000668.1:g.157528124A>G GRCh37
NC_000006.10:g.157569816A>G NCBI36
NG_032093.1:g.434061A>G
NG_032093.2:g.434061A>G
NG_066624.1:g.435965A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6218A>G MANE Select NP_001361757.1:p.Asn2073Ser
ENST00000636930.2:c.6218A>G MANE Select ENSP00000490491.2:p.Asn2073Ser
NM_001346813.1:c.5969A>G NP_001333742.1:p.Asn1990Ser
NM_001363725.1:c.3719A>G NP_001350654.1:p.Asn1240Ser
NM_001363725.2:c.3719A>G NP_001350654.1:p.Asn1240Ser
NM_001371656.1:c.6098A>G NP_001358585.1:p.Asn2033Ser
NM_001374820.1:c.6098A>G NP_001361749.1:p.Asn2033Ser
NM_017519.2:c.5810A>G NP_059989.2:p.Asn1937Ser
NM_017519.3:c.6059A>G NP_059989.3:p.Asn2020Ser
NM_020732.3:c.5849A>G NP_065783.3:p.Asn1950Ser
ENST00000346085.10:c.6098A>G ENSP00000344546.5:p.Asn2033Ser
ENST00000346085.9:c.5849A>G ENSP00000344546.4:p.Asn1950Ser
ENST00000350026.10:c.5810A>G ENSP00000055163.7:p.Asn1937Ser
ENST00000350026.11:c.6059A>G ENSP00000055163.8:p.Asn2020Ser
ENST00000350026.9:c.5810A>G ENSP00000055163.7:p.Asn1937Ser
ENST00000414678.6:c.4376A>G ENSP00000412835.2:p.Asn1459Ser
ENST00000414678.7:c.4376A>G ENSP00000412835.2:p.Asn1459Ser
ENST00000414678.8:c.6128A>G ENSP00000412835.3:p.Asn2043Ser
ENST00000635849.1:c.3539A>G ENSP00000490948.1:p.Asn1180Ser
ENST00000635928.1:c.374A>G ENSP00000489717.1:p.Asn125Ser
ENST00000635957.1:c.3170A>G ENSP00000490385.1:p.Asn1057Ser
ENST00000636227.1:n.4681A>G
ENST00000636254.1:n.2138A>G
ENST00000636940.1:n.4215A>G
ENST00000637015.1:c.3586A>G
ENST00000637015.2:c.6347A>G ENSP00000489729.2:p.Asn2116Ser
ENST00000637568.1:c.3500A>G
ENST00000637741.1:n.2884A>G
ENST00000637810.1:c.3560A>G ENSP00000489636.1:p.Asn1187Ser
ENST00000637904.1:c.3719A>G ENSP00000490550.1:p.Asn1240Ser
ENST00000637933.1:n.3333A>G
ENST00000647938.1:c.5849A>G ENSP00000498155.1:p.Asn1950Ser
XM_005267069.3:c.5969A>G XP_005267126.2:p.Asn1990Ser
XM_011535984.1:c.5048A>G XP_011534286.1:p.Asn1683Ser
XM_011535984.2:c.6179A>G XP_011534286.2:p.Asn2060Ser
XM_011535985.1:c.4868A>G XP_011534287.1:p.Asn1623Ser
XM_011535986.1:c.4628A>G XP_011534288.1:p.Asn1543Ser
XM_011535987.1:c.4247A>G XP_011534289.1:p.Asn1416Ser
XM_011535988.1:c.3110A>G XP_011534290.1:p.Asn1037Ser
XM_011535988.3:c.3110A>G XP_011534290.1:p.Asn1037Ser
XM_017011103.2:c.6080A>G XP_016866592.1:p.Asn2027Ser
XM_017011104.1:c.6050A>G XP_016866593.1:p.Asn2017Ser
XM_017011105.2:c.6020A>G XP_016866594.1:p.Asn2007Ser
XM_017011106.2:c.5891A>G XP_016866595.1:p.Asn1964Ser
XM_017011107.2:c.5870A>G XP_016866596.1:p.Asn1957Ser
XR_002956289.1:n.6165A>G