Canonical Allele Identifier: CA366248674
Community Standard Title: NM_001374828.1(ARID1B):c.6617T>C (p.Leu2206Pro)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157207389T>C , CM000668.2:g.157207389T>C GRCh38
NC_000006.11:g.157528523T>C , CM000668.1:g.157528523T>C GRCh37
NC_000006.10:g.157570215T>C NCBI36
NG_032093.1:g.434460T>C
NG_032093.2:g.434460T>C
NG_066624.1:g.436364T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6617T>C MANE Select NP_001361757.1:p.Leu2206Pro
ENST00000636930.2:c.6617T>C MANE Select ENSP00000490491.2:p.Leu2206Pro
NM_001346813.1:c.6368T>C NP_001333742.1:p.Leu2123Pro
NM_001363725.1:c.4118T>C NP_001350654.1:p.Leu1373Pro
NM_001363725.2:c.4118T>C NP_001350654.1:p.Leu1373Pro
NM_001371656.1:c.6497T>C NP_001358585.1:p.Leu2166Pro
NM_001374820.1:c.6497T>C NP_001361749.1:p.Leu2166Pro
NM_017519.2:c.6209T>C NP_059989.2:p.Leu2070Pro
NM_017519.3:c.6458T>C NP_059989.3:p.Leu2153Pro
NM_020732.3:c.6248T>C NP_065783.3:p.Leu2083Pro
ENST00000346085.10:c.6497T>C ENSP00000344546.5:p.Leu2166Pro
ENST00000346085.9:c.6248T>C ENSP00000344546.4:p.Leu2083Pro
ENST00000350026.10:c.6209T>C ENSP00000055163.7:p.Leu2070Pro
ENST00000350026.11:c.6458T>C ENSP00000055163.8:p.Leu2153Pro
ENST00000350026.9:c.6209T>C ENSP00000055163.7:p.Leu2070Pro
ENST00000414678.6:c.4775T>C ENSP00000412835.2:p.Leu1592Pro
ENST00000414678.7:c.4775T>C ENSP00000412835.2:p.Leu1592Pro
ENST00000414678.8:c.6527T>C ENSP00000412835.3:p.Leu2176Pro
ENST00000635849.1:c.3938T>C ENSP00000490948.1:p.Leu1313Pro
ENST00000635928.1:c.773T>C ENSP00000489717.1:p.Leu258Pro
ENST00000635957.1:c.3569T>C ENSP00000490385.1:p.Leu1190Pro
ENST00000636227.1:n.5080T>C
ENST00000636254.1:n.2537T>C
ENST00000636940.1:n.4614T>C
ENST00000637015.1:c.3985T>C
ENST00000637015.2:c.6746T>C ENSP00000489729.2:p.Leu2249Pro
ENST00000637568.1:c.3899T>C
ENST00000637741.1:n.3283T>C
ENST00000637810.1:c.3959T>C ENSP00000489636.1:p.Leu1320Pro
ENST00000637904.1:c.4118T>C ENSP00000490550.1:p.Leu1373Pro
ENST00000637933.1:n.3732T>C
ENST00000647938.1:c.6248T>C ENSP00000498155.1:p.Leu2083Pro
XM_005267069.3:c.6368T>C XP_005267126.2:p.Leu2123Pro
XM_011535984.1:c.5447T>C XP_011534286.1:p.Leu1816Pro
XM_011535984.2:c.6578T>C XP_011534286.2:p.Leu2193Pro
XM_011535985.1:c.5267T>C XP_011534287.1:p.Leu1756Pro
XM_011535986.1:c.5027T>C XP_011534288.1:p.Leu1676Pro
XM_011535987.1:c.4646T>C XP_011534289.1:p.Leu1549Pro
XM_011535988.1:c.3509T>C XP_011534290.1:p.Leu1170Pro
XM_011535988.3:c.3509T>C XP_011534290.1:p.Leu1170Pro
XM_017011103.2:c.6479T>C XP_016866592.1:p.Leu2160Pro
XM_017011104.1:c.6449T>C XP_016866593.1:p.Leu2150Pro
XM_017011105.2:c.6419T>C XP_016866594.1:p.Leu2140Pro
XM_017011106.2:c.6290T>C XP_016866595.1:p.Leu2097Pro
XM_017011107.2:c.6269T>C XP_016866596.1:p.Leu2090Pro
XR_002956289.1:n.6564T>C