Canonical Allele Identifier: CA366242340

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522389C>T (hg19) ; chr6:g.157201255C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201255C>T , CM000668.2:g.157201255C>T	GRCh38
NC_000006.11:g.157522389C>T , CM000668.1:g.157522389C>T	GRCh37
NC_000006.10:g.157564081C>T	NCBI36
NG_032093.1:g.428326C>T
NG_032093.2:g.428326C>T
NG_066624.1:g.430230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4871C>T	ENSP00000055163.8:p.Pro1624Leu
ENST00000414678.8:c.4940C>T	ENSP00000412835.3:p.Pro1647Leu
ENST00000637015.2:c.5159C>T	ENSP00000489729.2:p.Pro1720Leu
ENST00000346085.10:c.4910C>T	ENSP00000344546.5:p.Pro1637Leu
ENST00000350026.10:c.4622C>T	ENSP00000055163.7:p.Pro1541Leu
ENST00000414678.7:c.3188C>T	ENSP00000412835.2:p.Pro1063Leu
ENST00000635849.1:c.2351C>T	ENSP00000490948.1:p.Pro784Leu
ENST00000635957.1:c.1982C>T	ENSP00000490385.1:p.Pro661Leu
ENST00000636227.1:n.3493C>T
ENST00000636254.1:n.950C>T
ENST00000636930.2:c.5030C>T MANE Select	ENSP00000490491.2:p.Pro1677Leu
ENST00000636940.1:n.3027C>T
ENST00000637015.1:c.2398C>T
ENST00000637568.1:c.2312C>T
ENST00000637741.1:n.1696C>T
ENST00000637810.1:c.2372C>T	ENSP00000489636.1:p.Pro791Leu
ENST00000637904.1:c.2531C>T	ENSP00000490550.1:p.Pro844Leu
ENST00000647938.1:c.4661C>T	ENSP00000498155.1:p.Pro1554Leu
ENST00000346085.9:c.4661C>T	ENSP00000344546.4:p.Pro1554Leu
ENST00000350026.9:c.4622C>T	ENSP00000055163.7:p.Pro1541Leu
ENST00000414678.6:c.3188C>T	ENSP00000412835.2:p.Pro1063Leu
NM_017519.2:c.4622C>T	NP_059989.2:p.Pro1541Leu
NM_020732.3:c.4661C>T	NP_065783.3:p.Pro1554Leu
XM_005267069.3:c.4781C>T	XP_005267126.2:p.Pro1594Leu
XM_011535984.1:c.3860C>T	XP_011534286.1:p.Pro1287Leu
XM_011535985.1:c.3680C>T	XP_011534287.1:p.Pro1227Leu
XM_011535986.1:c.3440C>T	XP_011534288.1:p.Pro1147Leu
XM_011535987.1:c.3059C>T	XP_011534289.1:p.Pro1020Leu
XM_011535988.1:c.1922C>T	XP_011534290.1:p.Pro641Leu
NM_001346813.1:c.4781C>T	NP_001333742.1:p.Pro1594Leu
NM_001363725.1:c.2531C>T	NP_001350654.1:p.Pro844Leu
XM_011535984.2:c.4991C>T	XP_011534286.2:p.Pro1664Leu
XM_011535988.3:c.1922C>T	XP_011534290.1:p.Pro641Leu
XM_017011103.2:c.4892C>T	XP_016866592.1:p.Pro1631Leu
XM_017011104.1:c.4862C>T	XP_016866593.1:p.Pro1621Leu
XM_017011105.2:c.4832C>T	XP_016866594.1:p.Pro1611Leu
XM_017011106.2:c.4703C>T	XP_016866595.1:p.Pro1568Leu
XM_017011107.2:c.4682C>T	XP_016866596.1:p.Pro1561Leu
XR_002956289.1:n.4977C>T
NM_001363725.2:c.2531C>T	NP_001350654.1:p.Pro844Leu
NM_001371656.1:c.4910C>T	NP_001358585.1:p.Pro1637Leu
NM_001374820.1:c.4910C>T	NP_001361749.1:p.Pro1637Leu
NM_001374828.1:c.5030C>T MANE Select	NP_001361757.1:p.Pro1677Leu
NM_017519.3:c.4871C>T	NP_059989.3:p.Pro1624Leu