Canonical Allele Identifier: CA366241981

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374558
• gnomAD v4: 6-157201098-C-T
• MyVariant Identifiers: chr6:g.157522232C>T (hg19) ; chr6:g.157201098C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201098C>T , CM000668.2:g.157201098C>T	GRCh38
NC_000006.11:g.157522232C>T , CM000668.1:g.157522232C>T	GRCh37
NC_000006.10:g.157563924C>T	NCBI36
NG_032093.1:g.428169C>T
NG_032093.2:g.428169C>T
NG_066624.1:g.430073C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4714C>T	ENSP00000055163.8:p.Pro1572Ser
ENST00000414678.8:c.4783C>T	ENSP00000412835.3:p.Pro1595Ser
ENST00000637015.2:c.5002C>T	ENSP00000489729.2:p.Pro1668Ser
ENST00000346085.10:c.4753C>T	ENSP00000344546.5:p.Pro1585Ser
ENST00000350026.10:c.4465C>T	ENSP00000055163.7:p.Pro1489Ser
ENST00000414678.7:c.3031C>T	ENSP00000412835.2:p.Pro1011Ser
ENST00000635849.1:c.2194C>T	ENSP00000490948.1:p.Pro732Ser
ENST00000635957.1:c.1825C>T	ENSP00000490385.1:p.Pro609Ser
ENST00000636227.1:n.3336C>T
ENST00000636254.1:n.793C>T
ENST00000636930.2:c.4873C>T MANE Select	ENSP00000490491.2:p.Pro1625Ser
ENST00000636940.1:n.2870C>T
ENST00000637015.1:c.2241C>T
ENST00000637568.1:c.2155C>T
ENST00000637741.1:n.1539C>T
ENST00000637810.1:c.2215C>T	ENSP00000489636.1:p.Pro739Ser
ENST00000637904.1:c.2374C>T	ENSP00000490550.1:p.Pro792Ser
ENST00000647938.1:c.4504C>T	ENSP00000498155.1:p.Pro1502Ser
ENST00000346085.9:c.4504C>T	ENSP00000344546.4:p.Pro1502Ser
ENST00000350026.9:c.4465C>T	ENSP00000055163.7:p.Pro1489Ser
ENST00000414678.6:c.3031C>T	ENSP00000412835.2:p.Pro1011Ser
NM_017519.2:c.4465C>T	NP_059989.2:p.Pro1489Ser
NM_020732.3:c.4504C>T	NP_065783.3:p.Pro1502Ser
XM_005267069.3:c.4624C>T	XP_005267126.2:p.Pro1542Ser
XM_011535984.1:c.3703C>T	XP_011534286.1:p.Pro1235Ser
XM_011535985.1:c.3523C>T	XP_011534287.1:p.Pro1175Ser
XM_011535986.1:c.3283C>T	XP_011534288.1:p.Pro1095Ser
XM_011535987.1:c.2902C>T	XP_011534289.1:p.Pro968Ser
XM_011535988.1:c.1765C>T	XP_011534290.1:p.Pro589Ser
NM_001346813.1:c.4624C>T	NP_001333742.1:p.Pro1542Ser
NM_001363725.1:c.2374C>T	NP_001350654.1:p.Pro792Ser
XM_011535984.2:c.4834C>T	XP_011534286.2:p.Pro1612Ser
XM_011535988.3:c.1765C>T	XP_011534290.1:p.Pro589Ser
XM_017011103.2:c.4735C>T	XP_016866592.1:p.Pro1579Ser
XM_017011104.1:c.4705C>T	XP_016866593.1:p.Pro1569Ser
XM_017011105.2:c.4675C>T	XP_016866594.1:p.Pro1559Ser
XM_017011106.2:c.4546C>T	XP_016866595.1:p.Pro1516Ser
XM_017011107.2:c.4525C>T	XP_016866596.1:p.Pro1509Ser
XR_002956289.1:n.4820C>T
NM_001363725.2:c.2374C>T	NP_001350654.1:p.Pro792Ser
NM_001371656.1:c.4753C>T	NP_001358585.1:p.Pro1585Ser
NM_001374820.1:c.4753C>T	NP_001361749.1:p.Pro1585Ser
NM_001374828.1:c.4873C>T MANE Select	NP_001361757.1:p.Pro1625Ser
NM_017519.3:c.4714C>T	NP_059989.3:p.Pro1572Ser