Canonical Allele Identifier: CA366241688

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522179C>T (hg19) ; chr6:g.157201045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201045C>T , CM000668.2:g.157201045C>T	GRCh38
NC_000006.11:g.157522179C>T , CM000668.1:g.157522179C>T	GRCh37
NC_000006.10:g.157563871C>T	NCBI36
NG_032093.1:g.428116C>T
NG_032093.2:g.428116C>T
NG_066624.1:g.430020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4661C>T	ENSP00000055163.8:p.Pro1554Leu
ENST00000414678.8:c.4730C>T	ENSP00000412835.3:p.Pro1577Leu
ENST00000637015.2:c.4949C>T	ENSP00000489729.2:p.Pro1650Leu
ENST00000346085.10:c.4700C>T	ENSP00000344546.5:p.Pro1567Leu
ENST00000350026.10:c.4412C>T	ENSP00000055163.7:p.Pro1471Leu
ENST00000414678.7:c.2978C>T	ENSP00000412835.2:p.Pro993Leu
ENST00000635849.1:c.2141C>T	ENSP00000490948.1:p.Pro714Leu
ENST00000635957.1:c.1772C>T	ENSP00000490385.1:p.Pro591Leu
ENST00000636227.1:n.3283C>T
ENST00000636254.1:n.740C>T
ENST00000636930.2:c.4820C>T MANE Select	ENSP00000490491.2:p.Pro1607Leu
ENST00000636940.1:n.2817C>T
ENST00000637015.1:c.2188C>T
ENST00000637568.1:c.2102C>T
ENST00000637741.1:n.1486C>T
ENST00000637810.1:c.2162C>T	ENSP00000489636.1:p.Pro721Leu
ENST00000637904.1:c.2321C>T	ENSP00000490550.1:p.Pro774Leu
ENST00000647938.1:c.4451C>T	ENSP00000498155.1:p.Pro1484Leu
ENST00000346085.9:c.4451C>T	ENSP00000344546.4:p.Pro1484Leu
ENST00000350026.9:c.4412C>T	ENSP00000055163.7:p.Pro1471Leu
ENST00000414678.6:c.2978C>T	ENSP00000412835.2:p.Pro993Leu
NM_017519.2:c.4412C>T	NP_059989.2:p.Pro1471Leu
NM_020732.3:c.4451C>T	NP_065783.3:p.Pro1484Leu
XM_005267069.3:c.4571C>T	XP_005267126.2:p.Pro1524Leu
XM_011535984.1:c.3650C>T	XP_011534286.1:p.Pro1217Leu
XM_011535985.1:c.3470C>T	XP_011534287.1:p.Pro1157Leu
XM_011535986.1:c.3230C>T	XP_011534288.1:p.Pro1077Leu
XM_011535987.1:c.2849C>T	XP_011534289.1:p.Pro950Leu
XM_011535988.1:c.1712C>T	XP_011534290.1:p.Pro571Leu
NM_001346813.1:c.4571C>T	NP_001333742.1:p.Pro1524Leu
NM_001363725.1:c.2321C>T	NP_001350654.1:p.Pro774Leu
XM_011535984.2:c.4781C>T	XP_011534286.2:p.Pro1594Leu
XM_011535988.3:c.1712C>T	XP_011534290.1:p.Pro571Leu
XM_017011103.2:c.4682C>T	XP_016866592.1:p.Pro1561Leu
XM_017011104.1:c.4652C>T	XP_016866593.1:p.Pro1551Leu
XM_017011105.2:c.4622C>T	XP_016866594.1:p.Pro1541Leu
XM_017011106.2:c.4493C>T	XP_016866595.1:p.Pro1498Leu
XM_017011107.2:c.4472C>T	XP_016866596.1:p.Pro1491Leu
XR_002956289.1:n.4767C>T
NM_001363725.2:c.2321C>T	NP_001350654.1:p.Pro774Leu
NM_001371656.1:c.4700C>T	NP_001358585.1:p.Pro1567Leu
NM_001374820.1:c.4700C>T	NP_001361749.1:p.Pro1567Leu
NM_001374828.1:c.4820C>T MANE Select	NP_001361757.1:p.Pro1607Leu
NM_017519.3:c.4661C>T	NP_059989.3:p.Pro1554Leu