Canonical Allele Identifier: CA150362634

Gene: ARID1B

Linked Data

• dbSNP Id: rs768173199
• gnomAD v2: 6-157511051-T-A
• gnomAD v3: 6-157189917-T-A
• gnomAD v4: 6-157189917-T-A
• MyVariant Identifiers: chr6:g.157511051T>A (hg19) ; chr6:g.157189917T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189917T>A , CM000668.2:g.157189917T>A	GRCh38
NC_000006.11:g.157511051T>A , CM000668.1:g.157511051T>A	GRCh37
NC_000006.10:g.157552743T>A	NCBI36
NG_032093.1:g.416988T>A
NG_032093.2:g.416988T>A
NG_066624.1:g.418892T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-121T>A	ENSP00000055163.8:n.3900-121T>A
ENST00000414678.8:c.3969-121T>A	ENSP00000412835.3:n.3969-121T>A
ENST00000637015.2:c.4188-121T>A	ENSP00000489729.2:n.4188-121T>A
ENST00000346085.10:c.3939-121T>A	ENSP00000344546.5:n.3939-121T>A
ENST00000350026.10:c.3651-121T>A	ENSP00000055163.7:n.3651-121T>A
ENST00000414678.7:c.2217-121T>A	ENSP00000412835.2:n.2217-121T>A
ENST00000635849.1:c.1380-121T>A	ENSP00000490948.1:n.1380-121T>A
ENST00000635957.1:c.1014-124T>A	ENSP00000490385.1:n.1014-124T>A
ENST00000636930.2:c.4059-121T>A MANE Select	ENSP00000490491.2:n.4059-121T>A
ENST00000636940.1:n.2056-121T>A
ENST00000637015.1:c.1427-121T>A
ENST00000637568.1:c.1341-121T>A
ENST00000637741.1:n.725-121T>A
ENST00000637810.1:c.1401-121T>A	ENSP00000489636.1:n.1401-121T>A
ENST00000637904.1:c.1560-121T>A	ENSP00000490550.1:n.1560-121T>A
ENST00000647938.1:c.3690-121T>A	ENSP00000498155.1:n.3690-121T>A
ENST00000346085.9:c.3690-121T>A	ENSP00000344546.4:n.3690-121T>A
ENST00000350026.9:c.3651-121T>A	ENSP00000055163.7:n.3651-121T>A
ENST00000414678.6:c.2217-121T>A	ENSP00000412835.2:n.2217-121T>A
NM_017519.2:c.3651-121T>A	NP_059989.2:n.3651-121T>A
NM_020732.3:c.3690-121T>A	NP_065783.3:n.3690-121T>A
XM_005267069.3:c.3810-121T>A	XP_005267126.2:n.3810-121T>A
XM_011535984.1:c.2889-121T>A	XP_011534286.1:n.2889-121T>A
XM_011535985.1:c.2709-121T>A	XP_011534287.1:n.2709-121T>A
XM_011535986.1:c.2469-121T>A	XP_011534288.1:n.2469-121T>A
XM_011535987.1:c.2088-121T>A	XP_011534289.1:n.2088-121T>A
XM_011535988.1:c.951-121T>A	XP_011534290.1:n.951-121T>A
NM_001346813.1:c.3810-121T>A	NP_001333742.1:n.3810-121T>A
NM_001363725.1:c.1560-121T>A	NP_001350654.1:n.1560-121T>A
XM_011535984.2:c.4020-121T>A	XP_011534286.2:n.4020-121T>A
XM_011535988.3:c.951-121T>A	XP_011534290.1:n.951-121T>A
XM_017011103.2:c.3921-121T>A	XP_016866592.1:n.3921-121T>A
XM_017011104.1:c.3891-121T>A	XP_016866593.1:n.3891-121T>A
XM_017011105.2:c.3861-121T>A	XP_016866594.1:n.3861-121T>A
XM_017011106.2:c.3732-121T>A	XP_016866595.1:n.3732-121T>A
XM_017011107.2:c.3711-121T>A	XP_016866596.1:n.3711-121T>A
XR_002956289.1:n.4103-121T>A
NM_001363725.2:c.1560-121T>A	NP_001350654.1:n.1560-121T>A
NM_001371656.1:c.3939-121T>A	NP_001358585.1:n.3939-121T>A
NM_001374820.1:c.3939-121T>A	NP_001361749.1:n.3939-121T>A
NM_001374828.1:c.4059-121T>A MANE Select	NP_001361757.1:n.4059-121T>A
NM_017519.3:c.3900-121T>A	NP_059989.3:n.3900-121T>A