Canonical Allele Identifier: CA366242726

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1311074
• ClinVar RCV Id: RCV001758583
• dbSNP Id: rs781086610
• MyVariant Identifiers: chr6:g.157522491C>T (hg19) ; chr6:g.157201357C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4973C>T	ENSP00000055163.8:p.Pro1658Leu
ENST00000414678.8:c.5042C>T	ENSP00000412835.3:p.Pro1681Leu
ENST00000637015.2:c.5261C>T	ENSP00000489729.2:p.Pro1754Leu
ENST00000346085.10:c.5012C>T	ENSP00000344546.5:p.Pro1671Leu
ENST00000350026.10:c.4724C>T	ENSP00000055163.7:p.Pro1575Leu
ENST00000414678.7:c.3290C>T	ENSP00000412835.2:p.Pro1097Leu
ENST00000635849.1:c.2453C>T	ENSP00000490948.1:p.Pro818Leu
ENST00000635957.1:c.2084C>T	ENSP00000490385.1:p.Pro695Leu
ENST00000636227.1:n.3595C>T
ENST00000636254.1:n.1052C>T
ENST00000636930.2:c.5132C>T MANE Select	ENSP00000490491.2:p.Pro1711Leu
ENST00000636940.1:n.3129C>T
ENST00000637015.1:c.2500C>T
ENST00000637568.1:c.2414C>T
ENST00000637741.1:n.1798C>T
ENST00000637810.1:c.2474C>T	ENSP00000489636.1:p.Pro825Leu
ENST00000637904.1:c.2633C>T	ENSP00000490550.1:p.Pro878Leu
ENST00000647938.1:c.4763C>T	ENSP00000498155.1:p.Pro1588Leu
ENST00000346085.9:c.4763C>T	ENSP00000344546.4:p.Pro1588Leu
ENST00000350026.9:c.4724C>T	ENSP00000055163.7:p.Pro1575Leu
ENST00000414678.6:c.3290C>T	ENSP00000412835.2:p.Pro1097Leu
NM_017519.2:c.4724C>T	NP_059989.2:p.Pro1575Leu
NM_020732.3:c.4763C>T	NP_065783.3:p.Pro1588Leu
XM_005267069.3:c.4883C>T	XP_005267126.2:p.Pro1628Leu
XM_011535984.1:c.3962C>T	XP_011534286.1:p.Pro1321Leu
XM_011535985.1:c.3782C>T	XP_011534287.1:p.Pro1261Leu
XM_011535986.1:c.3542C>T	XP_011534288.1:p.Pro1181Leu
XM_011535987.1:c.3161C>T	XP_011534289.1:p.Pro1054Leu
XM_011535988.1:c.2024C>T	XP_011534290.1:p.Pro675Leu
NM_001346813.1:c.4883C>T	NP_001333742.1:p.Pro1628Leu
NM_001363725.1:c.2633C>T	NP_001350654.1:p.Pro878Leu
XM_011535984.2:c.5093C>T	XP_011534286.2:p.Pro1698Leu
XM_011535988.3:c.2024C>T	XP_011534290.1:p.Pro675Leu
XM_017011103.2:c.4994C>T	XP_016866592.1:p.Pro1665Leu
XM_017011104.1:c.4964C>T	XP_016866593.1:p.Pro1655Leu
XM_017011105.2:c.4934C>T	XP_016866594.1:p.Pro1645Leu
XM_017011106.2:c.4805C>T	XP_016866595.1:p.Pro1602Leu
XM_017011107.2:c.4784C>T	XP_016866596.1:p.Pro1595Leu
XR_002956289.1:n.5079C>T
NM_001363725.2:c.2633C>T	NP_001350654.1:p.Pro878Leu
NM_001371656.1:c.5012C>T	NP_001358585.1:p.Pro1671Leu
NM_001374820.1:c.5012C>T	NP_001361749.1:p.Pro1671Leu
NM_001374828.1:c.5132C>T MANE Select	NP_001361757.1:p.Pro1711Leu
NM_017519.3:c.4973C>T	NP_059989.3:p.Pro1658Leu