Canonical Allele Identifier: CA366242911

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522530C>A (hg19) ; chr6:g.157201396C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201396C>A , CM000668.2:g.157201396C>A	GRCh38
NC_000006.11:g.157522530C>A , CM000668.1:g.157522530C>A	GRCh37
NC_000006.10:g.157564222C>A	NCBI36
NG_032093.1:g.428467C>A
NG_032093.2:g.428467C>A
NG_066624.1:g.430371C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5012C>A	ENSP00000055163.8:p.Pro1671Gln
ENST00000414678.8:c.5081C>A	ENSP00000412835.3:p.Pro1694Gln
ENST00000637015.2:c.5300C>A	ENSP00000489729.2:p.Pro1767Gln
ENST00000346085.10:c.5051C>A	ENSP00000344546.5:p.Pro1684Gln
ENST00000350026.10:c.4763C>A	ENSP00000055163.7:p.Pro1588Gln
ENST00000414678.7:c.3329C>A	ENSP00000412835.2:p.Pro1110Gln
ENST00000635849.1:c.2492C>A	ENSP00000490948.1:p.Pro831Gln
ENST00000635957.1:c.2123C>A	ENSP00000490385.1:p.Pro708Gln
ENST00000636227.1:n.3634C>A
ENST00000636254.1:n.1091C>A
ENST00000636930.2:c.5171C>A MANE Select	ENSP00000490491.2:p.Pro1724Gln
ENST00000636940.1:n.3168C>A
ENST00000637015.1:c.2539C>A
ENST00000637568.1:c.2453C>A
ENST00000637741.1:n.1837C>A
ENST00000637810.1:c.2513C>A	ENSP00000489636.1:p.Pro838Gln
ENST00000637904.1:c.2672C>A	ENSP00000490550.1:p.Pro891Gln
ENST00000647938.1:c.4802C>A	ENSP00000498155.1:p.Pro1601Gln
ENST00000346085.9:c.4802C>A	ENSP00000344546.4:p.Pro1601Gln
ENST00000350026.9:c.4763C>A	ENSP00000055163.7:p.Pro1588Gln
ENST00000414678.6:c.3329C>A	ENSP00000412835.2:p.Pro1110Gln
NM_017519.2:c.4763C>A	NP_059989.2:p.Pro1588Gln
NM_020732.3:c.4802C>A	NP_065783.3:p.Pro1601Gln
XM_005267069.3:c.4922C>A	XP_005267126.2:p.Pro1641Gln
XM_011535984.1:c.4001C>A	XP_011534286.1:p.Pro1334Gln
XM_011535985.1:c.3821C>A	XP_011534287.1:p.Pro1274Gln
XM_011535986.1:c.3581C>A	XP_011534288.1:p.Pro1194Gln
XM_011535987.1:c.3200C>A	XP_011534289.1:p.Pro1067Gln
XM_011535988.1:c.2063C>A	XP_011534290.1:p.Pro688Gln
NM_001346813.1:c.4922C>A	NP_001333742.1:p.Pro1641Gln
NM_001363725.1:c.2672C>A	NP_001350654.1:p.Pro891Gln
XM_011535984.2:c.5132C>A	XP_011534286.2:p.Pro1711Gln
XM_011535988.3:c.2063C>A	XP_011534290.1:p.Pro688Gln
XM_017011103.2:c.5033C>A	XP_016866592.1:p.Pro1678Gln
XM_017011104.1:c.5003C>A	XP_016866593.1:p.Pro1668Gln
XM_017011105.2:c.4973C>A	XP_016866594.1:p.Pro1658Gln
XM_017011106.2:c.4844C>A	XP_016866595.1:p.Pro1615Gln
XM_017011107.2:c.4823C>A	XP_016866596.1:p.Pro1608Gln
XR_002956289.1:n.5118C>A
NM_001363725.2:c.2672C>A	NP_001350654.1:p.Pro891Gln
NM_001371656.1:c.5051C>A	NP_001358585.1:p.Pro1684Gln
NM_001374820.1:c.5051C>A	NP_001361749.1:p.Pro1684Gln
NM_001374828.1:c.5171C>A MANE Select	NP_001361757.1:p.Pro1724Gln
NM_017519.3:c.5012C>A	NP_059989.3:p.Pro1671Gln