Canonical Allele Identifier: CA366239760

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366350
• MyVariant Identifiers: chr6:g.157519997C>G (hg19) ; chr6:g.157198863C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198863C>G , CM000668.2:g.157198863C>G	GRCh38
NC_000006.11:g.157519997C>G , CM000668.1:g.157519997C>G	GRCh37
NC_000006.10:g.157561689C>G	NCBI36
NG_032093.1:g.425934C>G
NG_032093.2:g.425934C>G
NG_066624.1:g.427838C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4276C>G	ENSP00000055163.8:p.Pro1426Ala
ENST00000414678.8:c.4345C>G	ENSP00000412835.3:p.Pro1449Ala
ENST00000637015.2:c.4564C>G	ENSP00000489729.2:p.Pro1522Ala
ENST00000346085.10:c.4315C>G	ENSP00000344546.5:p.Pro1439Ala
ENST00000350026.10:c.4027C>G	ENSP00000055163.7:p.Pro1343Ala
ENST00000414678.7:c.2593C>G	ENSP00000412835.2:p.Pro865Ala
ENST00000635849.1:c.1756C>G	ENSP00000490948.1:p.Pro586Ala
ENST00000635957.1:c.1387C>G	ENSP00000490385.1:p.Pro463Ala
ENST00000636227.1:n.2898C>G
ENST00000636254.1:n.355C>G
ENST00000636930.2:c.4435C>G MANE Select	ENSP00000490491.2:p.Pro1479Ala
ENST00000636940.1:n.2432C>G
ENST00000637015.1:c.1803C>G
ENST00000637568.1:c.1717C>G
ENST00000637741.1:n.1101C>G
ENST00000637810.1:c.1777C>G	ENSP00000489636.1:p.Pro593Ala
ENST00000637904.1:c.1936C>G	ENSP00000490550.1:p.Pro646Ala
ENST00000647938.1:c.4066C>G	ENSP00000498155.1:p.Pro1356Ala
ENST00000346085.9:c.4066C>G	ENSP00000344546.4:p.Pro1356Ala
ENST00000350026.9:c.4027C>G	ENSP00000055163.7:p.Pro1343Ala
ENST00000414678.6:c.2593C>G	ENSP00000412835.2:p.Pro865Ala
NM_017519.2:c.4027C>G	NP_059989.2:p.Pro1343Ala
NM_020732.3:c.4066C>G	NP_065783.3:p.Pro1356Ala
XM_005267069.3:c.4186C>G	XP_005267126.2:p.Pro1396Ala
XM_011535984.1:c.3265C>G	XP_011534286.1:p.Pro1089Ala
XM_011535985.1:c.3085C>G	XP_011534287.1:p.Pro1029Ala
XM_011535986.1:c.2845C>G	XP_011534288.1:p.Pro949Ala
XM_011535987.1:c.2464C>G	XP_011534289.1:p.Pro822Ala
XM_011535988.1:c.1327C>G	XP_011534290.1:p.Pro443Ala
NM_001346813.1:c.4186C>G	NP_001333742.1:p.Pro1396Ala
NM_001363725.1:c.1936C>G	NP_001350654.1:p.Pro646Ala
XM_011535984.2:c.4396C>G	XP_011534286.2:p.Pro1466Ala
XM_011535988.3:c.1327C>G	XP_011534290.1:p.Pro443Ala
XM_017011103.2:c.4297C>G	XP_016866592.1:p.Pro1433Ala
XM_017011104.1:c.4267C>G	XP_016866593.1:p.Pro1423Ala
XM_017011105.2:c.4237C>G	XP_016866594.1:p.Pro1413Ala
XM_017011106.2:c.4108C>G	XP_016866595.1:p.Pro1370Ala
XM_017011107.2:c.4087C>G	XP_016866596.1:p.Pro1363Ala
XR_002956289.1:n.4427-1842C>G
NM_001363725.2:c.1936C>G	NP_001350654.1:p.Pro646Ala
NM_001371656.1:c.4315C>G	NP_001358585.1:p.Pro1439Ala
NM_001374820.1:c.4315C>G	NP_001361749.1:p.Pro1439Ala
NM_001374828.1:c.4435C>G MANE Select	NP_001361757.1:p.Pro1479Ala
NM_017519.3:c.4276C>G	NP_059989.3:p.Pro1426Ala