Canonical Allele Identifier: CA366242851

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522518C>T (hg19) ; chr6:g.157201384C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201384C>T , CM000668.2:g.157201384C>T	GRCh38
NC_000006.11:g.157522518C>T , CM000668.1:g.157522518C>T	GRCh37
NC_000006.10:g.157564210C>T	NCBI36
NG_032093.1:g.428455C>T
NG_032093.2:g.428455C>T
NG_066624.1:g.430359C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5000C>T	ENSP00000055163.8:p.Pro1667Leu
ENST00000414678.8:c.5069C>T	ENSP00000412835.3:p.Pro1690Leu
ENST00000637015.2:c.5288C>T	ENSP00000489729.2:p.Pro1763Leu
ENST00000346085.10:c.5039C>T	ENSP00000344546.5:p.Pro1680Leu
ENST00000350026.10:c.4751C>T	ENSP00000055163.7:p.Pro1584Leu
ENST00000414678.7:c.3317C>T	ENSP00000412835.2:p.Pro1106Leu
ENST00000635849.1:c.2480C>T	ENSP00000490948.1:p.Pro827Leu
ENST00000635957.1:c.2111C>T	ENSP00000490385.1:p.Pro704Leu
ENST00000636227.1:n.3622C>T
ENST00000636254.1:n.1079C>T
ENST00000636930.2:c.5159C>T MANE Select	ENSP00000490491.2:p.Pro1720Leu
ENST00000636940.1:n.3156C>T
ENST00000637015.1:c.2527C>T
ENST00000637568.1:c.2441C>T
ENST00000637741.1:n.1825C>T
ENST00000637810.1:c.2501C>T	ENSP00000489636.1:p.Pro834Leu
ENST00000637904.1:c.2660C>T	ENSP00000490550.1:p.Pro887Leu
ENST00000647938.1:c.4790C>T	ENSP00000498155.1:p.Pro1597Leu
ENST00000346085.9:c.4790C>T	ENSP00000344546.4:p.Pro1597Leu
ENST00000350026.9:c.4751C>T	ENSP00000055163.7:p.Pro1584Leu
ENST00000414678.6:c.3317C>T	ENSP00000412835.2:p.Pro1106Leu
NM_017519.2:c.4751C>T	NP_059989.2:p.Pro1584Leu
NM_020732.3:c.4790C>T	NP_065783.3:p.Pro1597Leu
XM_005267069.3:c.4910C>T	XP_005267126.2:p.Pro1637Leu
XM_011535984.1:c.3989C>T	XP_011534286.1:p.Pro1330Leu
XM_011535985.1:c.3809C>T	XP_011534287.1:p.Pro1270Leu
XM_011535986.1:c.3569C>T	XP_011534288.1:p.Pro1190Leu
XM_011535987.1:c.3188C>T	XP_011534289.1:p.Pro1063Leu
XM_011535988.1:c.2051C>T	XP_011534290.1:p.Pro684Leu
NM_001346813.1:c.4910C>T	NP_001333742.1:p.Pro1637Leu
NM_001363725.1:c.2660C>T	NP_001350654.1:p.Pro887Leu
XM_011535984.2:c.5120C>T	XP_011534286.2:p.Pro1707Leu
XM_011535988.3:c.2051C>T	XP_011534290.1:p.Pro684Leu
XM_017011103.2:c.5021C>T	XP_016866592.1:p.Pro1674Leu
XM_017011104.1:c.4991C>T	XP_016866593.1:p.Pro1664Leu
XM_017011105.2:c.4961C>T	XP_016866594.1:p.Pro1654Leu
XM_017011106.2:c.4832C>T	XP_016866595.1:p.Pro1611Leu
XM_017011107.2:c.4811C>T	XP_016866596.1:p.Pro1604Leu
XR_002956289.1:n.5106C>T
NM_001363725.2:c.2660C>T	NP_001350654.1:p.Pro887Leu
NM_001371656.1:c.5039C>T	NP_001358585.1:p.Pro1680Leu
NM_001374820.1:c.5039C>T	NP_001361749.1:p.Pro1680Leu
NM_001374828.1:c.5159C>T MANE Select	NP_001361757.1:p.Pro1720Leu
NM_017519.3:c.5000C>T	NP_059989.3:p.Pro1667Leu