Canonical Allele Identifier: CA366242109

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201147-A-G
• MyVariant Identifiers: chr6:g.157522281A>G (hg19) ; chr6:g.157201147A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201147A>G , CM000668.2:g.157201147A>G	GRCh38
NC_000006.11:g.157522281A>G , CM000668.1:g.157522281A>G	GRCh37
NC_000006.10:g.157563973A>G	NCBI36
NG_032093.1:g.428218A>G
NG_032093.2:g.428218A>G
NG_066624.1:g.430122A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4763A>G	ENSP00000055163.8:p.Gln1588Arg
ENST00000414678.8:c.4832A>G	ENSP00000412835.3:p.Gln1611Arg
ENST00000637015.2:c.5051A>G	ENSP00000489729.2:p.Gln1684Arg
ENST00000346085.10:c.4802A>G	ENSP00000344546.5:p.Gln1601Arg
ENST00000350026.10:c.4514A>G	ENSP00000055163.7:p.Gln1505Arg
ENST00000414678.7:c.3080A>G	ENSP00000412835.2:p.Gln1027Arg
ENST00000635849.1:c.2243A>G	ENSP00000490948.1:p.Gln748Arg
ENST00000635957.1:c.1874A>G	ENSP00000490385.1:p.Gln625Arg
ENST00000636227.1:n.3385A>G
ENST00000636254.1:n.842A>G
ENST00000636930.2:c.4922A>G MANE Select	ENSP00000490491.2:p.Gln1641Arg
ENST00000636940.1:n.2919A>G
ENST00000637015.1:c.2290A>G
ENST00000637568.1:c.2204A>G
ENST00000637741.1:n.1588A>G
ENST00000637810.1:c.2264A>G	ENSP00000489636.1:p.Gln755Arg
ENST00000637904.1:c.2423A>G	ENSP00000490550.1:p.Gln808Arg
ENST00000647938.1:c.4553A>G	ENSP00000498155.1:p.Gln1518Arg
ENST00000346085.9:c.4553A>G	ENSP00000344546.4:p.Gln1518Arg
ENST00000350026.9:c.4514A>G	ENSP00000055163.7:p.Gln1505Arg
ENST00000414678.6:c.3080A>G	ENSP00000412835.2:p.Gln1027Arg
NM_017519.2:c.4514A>G	NP_059989.2:p.Gln1505Arg
NM_020732.3:c.4553A>G	NP_065783.3:p.Gln1518Arg
XM_005267069.3:c.4673A>G	XP_005267126.2:p.Gln1558Arg
XM_011535984.1:c.3752A>G	XP_011534286.1:p.Gln1251Arg
XM_011535985.1:c.3572A>G	XP_011534287.1:p.Gln1191Arg
XM_011535986.1:c.3332A>G	XP_011534288.1:p.Gln1111Arg
XM_011535987.1:c.2951A>G	XP_011534289.1:p.Gln984Arg
XM_011535988.1:c.1814A>G	XP_011534290.1:p.Gln605Arg
NM_001346813.1:c.4673A>G	NP_001333742.1:p.Gln1558Arg
NM_001363725.1:c.2423A>G	NP_001350654.1:p.Gln808Arg
XM_011535984.2:c.4883A>G	XP_011534286.2:p.Gln1628Arg
XM_011535988.3:c.1814A>G	XP_011534290.1:p.Gln605Arg
XM_017011103.2:c.4784A>G	XP_016866592.1:p.Gln1595Arg
XM_017011104.1:c.4754A>G	XP_016866593.1:p.Gln1585Arg
XM_017011105.2:c.4724A>G	XP_016866594.1:p.Gln1575Arg
XM_017011106.2:c.4595A>G	XP_016866595.1:p.Gln1532Arg
XM_017011107.2:c.4574A>G	XP_016866596.1:p.Gln1525Arg
XR_002956289.1:n.4869A>G
NM_001363725.2:c.2423A>G	NP_001350654.1:p.Gln808Arg
NM_001371656.1:c.4802A>G	NP_001358585.1:p.Gln1601Arg
NM_001374820.1:c.4802A>G	NP_001361749.1:p.Gln1601Arg
NM_001374828.1:c.4922A>G MANE Select	NP_001361757.1:p.Gln1641Arg
NM_017519.3:c.4763A>G	NP_059989.3:p.Gln1588Arg