Canonical Allele Identifier: CA366242916

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5012C>G	ENSP00000055163.8:p.Pro1671Arg
ENST00000414678.8:c.5081C>G	ENSP00000412835.3:p.Pro1694Arg
ENST00000637015.2:c.5300C>G	ENSP00000489729.2:p.Pro1767Arg
ENST00000346085.10:c.5051C>G	ENSP00000344546.5:p.Pro1684Arg
ENST00000350026.10:c.4763C>G	ENSP00000055163.7:p.Pro1588Arg
ENST00000414678.7:c.3329C>G	ENSP00000412835.2:p.Pro1110Arg
ENST00000635849.1:c.2492C>G	ENSP00000490948.1:p.Pro831Arg
ENST00000635957.1:c.2123C>G	ENSP00000490385.1:p.Pro708Arg
ENST00000636227.1:n.3634C>G
ENST00000636254.1:n.1091C>G
ENST00000636930.2:c.5171C>G MANE Select	ENSP00000490491.2:p.Pro1724Arg
ENST00000636940.1:n.3168C>G
ENST00000637015.1:c.2539C>G
ENST00000637568.1:c.2453C>G
ENST00000637741.1:n.1837C>G
ENST00000637810.1:c.2513C>G	ENSP00000489636.1:p.Pro838Arg
ENST00000637904.1:c.2672C>G	ENSP00000490550.1:p.Pro891Arg
ENST00000647938.1:c.4802C>G	ENSP00000498155.1:p.Pro1601Arg
ENST00000346085.9:c.4802C>G	ENSP00000344546.4:p.Pro1601Arg
ENST00000350026.9:c.4763C>G	ENSP00000055163.7:p.Pro1588Arg
ENST00000414678.6:c.3329C>G	ENSP00000412835.2:p.Pro1110Arg
NM_017519.2:c.4763C>G	NP_059989.2:p.Pro1588Arg
NM_020732.3:c.4802C>G	NP_065783.3:p.Pro1601Arg
XM_005267069.3:c.4922C>G	XP_005267126.2:p.Pro1641Arg
XM_011535984.1:c.4001C>G	XP_011534286.1:p.Pro1334Arg
XM_011535985.1:c.3821C>G	XP_011534287.1:p.Pro1274Arg
XM_011535986.1:c.3581C>G	XP_011534288.1:p.Pro1194Arg
XM_011535987.1:c.3200C>G	XP_011534289.1:p.Pro1067Arg
XM_011535988.1:c.2063C>G	XP_011534290.1:p.Pro688Arg
NM_001346813.1:c.4922C>G	NP_001333742.1:p.Pro1641Arg
NM_001363725.1:c.2672C>G	NP_001350654.1:p.Pro891Arg
XM_011535984.2:c.5132C>G	XP_011534286.2:p.Pro1711Arg
XM_011535988.3:c.2063C>G	XP_011534290.1:p.Pro688Arg
XM_017011103.2:c.5033C>G	XP_016866592.1:p.Pro1678Arg
XM_017011104.1:c.5003C>G	XP_016866593.1:p.Pro1668Arg
XM_017011105.2:c.4973C>G	XP_016866594.1:p.Pro1658Arg
XM_017011106.2:c.4844C>G	XP_016866595.1:p.Pro1615Arg
XM_017011107.2:c.4823C>G	XP_016866596.1:p.Pro1608Arg
XR_002956289.1:n.5118C>G
NM_001363725.2:c.2672C>G	NP_001350654.1:p.Pro891Arg
NM_001371656.1:c.5051C>G	NP_001358585.1:p.Pro1684Arg
NM_001374820.1:c.5051C>G	NP_001361749.1:p.Pro1684Arg
NM_001374828.1:c.5171C>G MANE Select	NP_001361757.1:p.Pro1724Arg
NM_017519.3:c.5012C>G	NP_059989.3:p.Pro1671Arg