Canonical Allele Identifier: CA366242724

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522491C>A (hg19) ; chr6:g.157201357C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201357C>A , CM000668.2:g.157201357C>A	GRCh38
NC_000006.11:g.157522491C>A , CM000668.1:g.157522491C>A	GRCh37
NC_000006.10:g.157564183C>A	NCBI36
NG_032093.1:g.428428C>A
NG_032093.2:g.428428C>A
NG_066624.1:g.430332C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4973C>A	ENSP00000055163.8:p.Pro1658His
ENST00000414678.8:c.5042C>A	ENSP00000412835.3:p.Pro1681His
ENST00000637015.2:c.5261C>A	ENSP00000489729.2:p.Pro1754His
ENST00000346085.10:c.5012C>A	ENSP00000344546.5:p.Pro1671His
ENST00000350026.10:c.4724C>A	ENSP00000055163.7:p.Pro1575His
ENST00000414678.7:c.3290C>A	ENSP00000412835.2:p.Pro1097His
ENST00000635849.1:c.2453C>A	ENSP00000490948.1:p.Pro818His
ENST00000635957.1:c.2084C>A	ENSP00000490385.1:p.Pro695His
ENST00000636227.1:n.3595C>A
ENST00000636254.1:n.1052C>A
ENST00000636930.2:c.5132C>A MANE Select	ENSP00000490491.2:p.Pro1711His
ENST00000636940.1:n.3129C>A
ENST00000637015.1:c.2500C>A
ENST00000637568.1:c.2414C>A
ENST00000637741.1:n.1798C>A
ENST00000637810.1:c.2474C>A	ENSP00000489636.1:p.Pro825His
ENST00000637904.1:c.2633C>A	ENSP00000490550.1:p.Pro878His
ENST00000647938.1:c.4763C>A	ENSP00000498155.1:p.Pro1588His
ENST00000346085.9:c.4763C>A	ENSP00000344546.4:p.Pro1588His
ENST00000350026.9:c.4724C>A	ENSP00000055163.7:p.Pro1575His
ENST00000414678.6:c.3290C>A	ENSP00000412835.2:p.Pro1097His
NM_017519.2:c.4724C>A	NP_059989.2:p.Pro1575His
NM_020732.3:c.4763C>A	NP_065783.3:p.Pro1588His
XM_005267069.3:c.4883C>A	XP_005267126.2:p.Pro1628His
XM_011535984.1:c.3962C>A	XP_011534286.1:p.Pro1321His
XM_011535985.1:c.3782C>A	XP_011534287.1:p.Pro1261His
XM_011535986.1:c.3542C>A	XP_011534288.1:p.Pro1181His
XM_011535987.1:c.3161C>A	XP_011534289.1:p.Pro1054His
XM_011535988.1:c.2024C>A	XP_011534290.1:p.Pro675His
NM_001346813.1:c.4883C>A	NP_001333742.1:p.Pro1628His
NM_001363725.1:c.2633C>A	NP_001350654.1:p.Pro878His
XM_011535984.2:c.5093C>A	XP_011534286.2:p.Pro1698His
XM_011535988.3:c.2024C>A	XP_011534290.1:p.Pro675His
XM_017011103.2:c.4994C>A	XP_016866592.1:p.Pro1665His
XM_017011104.1:c.4964C>A	XP_016866593.1:p.Pro1655His
XM_017011105.2:c.4934C>A	XP_016866594.1:p.Pro1645His
XM_017011106.2:c.4805C>A	XP_016866595.1:p.Pro1602His
XM_017011107.2:c.4784C>A	XP_016866596.1:p.Pro1595His
XR_002956289.1:n.5079C>A
NM_001363725.2:c.2633C>A	NP_001350654.1:p.Pro878His
NM_001371656.1:c.5012C>A	NP_001358585.1:p.Pro1671His
NM_001374820.1:c.5012C>A	NP_001361749.1:p.Pro1671His
NM_001374828.1:c.5132C>A MANE Select	NP_001361757.1:p.Pro1711His
NM_017519.3:c.4973C>A	NP_059989.3:p.Pro1658His