Canonical Allele Identifier: CA366242285

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522362C>T (hg19) ; chr6:g.157201228C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201228C>T , CM000668.2:g.157201228C>T	GRCh38
NC_000006.11:g.157522362C>T , CM000668.1:g.157522362C>T	GRCh37
NC_000006.10:g.157564054C>T	NCBI36
NG_032093.1:g.428299C>T
NG_032093.2:g.428299C>T
NG_066624.1:g.430203C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4844C>T	ENSP00000055163.8:p.Ser1615Leu
ENST00000414678.8:c.4913C>T	ENSP00000412835.3:p.Ser1638Leu
ENST00000637015.2:c.5132C>T	ENSP00000489729.2:p.Ser1711Leu
ENST00000346085.10:c.4883C>T	ENSP00000344546.5:p.Ser1628Leu
ENST00000350026.10:c.4595C>T	ENSP00000055163.7:p.Ser1532Leu
ENST00000414678.7:c.3161C>T	ENSP00000412835.2:p.Ser1054Leu
ENST00000635849.1:c.2324C>T	ENSP00000490948.1:p.Ser775Leu
ENST00000635957.1:c.1955C>T	ENSP00000490385.1:p.Ser652Leu
ENST00000636227.1:n.3466C>T
ENST00000636254.1:n.923C>T
ENST00000636930.2:c.5003C>T MANE Select	ENSP00000490491.2:p.Ser1668Leu
ENST00000636940.1:n.3000C>T
ENST00000637015.1:c.2371C>T
ENST00000637568.1:c.2285C>T
ENST00000637741.1:n.1669C>T
ENST00000637810.1:c.2345C>T	ENSP00000489636.1:p.Ser782Leu
ENST00000637904.1:c.2504C>T	ENSP00000490550.1:p.Ser835Leu
ENST00000647938.1:c.4634C>T	ENSP00000498155.1:p.Ser1545Leu
ENST00000346085.9:c.4634C>T	ENSP00000344546.4:p.Ser1545Leu
ENST00000350026.9:c.4595C>T	ENSP00000055163.7:p.Ser1532Leu
ENST00000414678.6:c.3161C>T	ENSP00000412835.2:p.Ser1054Leu
NM_017519.2:c.4595C>T	NP_059989.2:p.Ser1532Leu
NM_020732.3:c.4634C>T	NP_065783.3:p.Ser1545Leu
XM_005267069.3:c.4754C>T	XP_005267126.2:p.Ser1585Leu
XM_011535984.1:c.3833C>T	XP_011534286.1:p.Ser1278Leu
XM_011535985.1:c.3653C>T	XP_011534287.1:p.Ser1218Leu
XM_011535986.1:c.3413C>T	XP_011534288.1:p.Ser1138Leu
XM_011535987.1:c.3032C>T	XP_011534289.1:p.Ser1011Leu
XM_011535988.1:c.1895C>T	XP_011534290.1:p.Ser632Leu
NM_001346813.1:c.4754C>T	NP_001333742.1:p.Ser1585Leu
NM_001363725.1:c.2504C>T	NP_001350654.1:p.Ser835Leu
XM_011535984.2:c.4964C>T	XP_011534286.2:p.Ser1655Leu
XM_011535988.3:c.1895C>T	XP_011534290.1:p.Ser632Leu
XM_017011103.2:c.4865C>T	XP_016866592.1:p.Ser1622Leu
XM_017011104.1:c.4835C>T	XP_016866593.1:p.Ser1612Leu
XM_017011105.2:c.4805C>T	XP_016866594.1:p.Ser1602Leu
XM_017011106.2:c.4676C>T	XP_016866595.1:p.Ser1559Leu
XM_017011107.2:c.4655C>T	XP_016866596.1:p.Ser1552Leu
XR_002956289.1:n.4950C>T
NM_001363725.2:c.2504C>T	NP_001350654.1:p.Ser835Leu
NM_001371656.1:c.4883C>T	NP_001358585.1:p.Ser1628Leu
NM_001374820.1:c.4883C>T	NP_001361749.1:p.Ser1628Leu
NM_001374828.1:c.5003C>T MANE Select	NP_001361757.1:p.Ser1668Leu
NM_017519.3:c.4844C>T	NP_059989.3:p.Ser1615Leu