Canonical Allele Identifier: CA366242197

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 3009335
• ClinVar RCV Id: RCV003869486
• dbSNP Id: rs2128375144
• MyVariant Identifiers: chr6:g.157522319C>T (hg19) ; chr6:g.157201185C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201185C>T , CM000668.2:g.157201185C>T	GRCh38
NC_000006.11:g.157522319C>T , CM000668.1:g.157522319C>T	GRCh37
NC_000006.10:g.157564011C>T	NCBI36
NG_032093.1:g.428256C>T
NG_032093.2:g.428256C>T
NG_066624.1:g.430160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4801C>T	ENSP00000055163.8:p.Pro1601Ser
ENST00000414678.8:c.4870C>T	ENSP00000412835.3:p.Pro1624Ser
ENST00000637015.2:c.5089C>T	ENSP00000489729.2:p.Pro1697Ser
ENST00000346085.10:c.4840C>T	ENSP00000344546.5:p.Pro1614Ser
ENST00000350026.10:c.4552C>T	ENSP00000055163.7:p.Pro1518Ser
ENST00000414678.7:c.3118C>T	ENSP00000412835.2:p.Pro1040Ser
ENST00000635849.1:c.2281C>T	ENSP00000490948.1:p.Pro761Ser
ENST00000635957.1:c.1912C>T	ENSP00000490385.1:p.Pro638Ser
ENST00000636227.1:n.3423C>T
ENST00000636254.1:n.880C>T
ENST00000636930.2:c.4960C>T MANE Select	ENSP00000490491.2:p.Pro1654Ser
ENST00000636940.1:n.2957C>T
ENST00000637015.1:c.2328C>T
ENST00000637568.1:c.2242C>T
ENST00000637741.1:n.1626C>T
ENST00000637810.1:c.2302C>T	ENSP00000489636.1:p.Pro768Ser
ENST00000637904.1:c.2461C>T	ENSP00000490550.1:p.Pro821Ser
ENST00000647938.1:c.4591C>T	ENSP00000498155.1:p.Pro1531Ser
ENST00000346085.9:c.4591C>T	ENSP00000344546.4:p.Pro1531Ser
ENST00000350026.9:c.4552C>T	ENSP00000055163.7:p.Pro1518Ser
ENST00000414678.6:c.3118C>T	ENSP00000412835.2:p.Pro1040Ser
NM_017519.2:c.4552C>T	NP_059989.2:p.Pro1518Ser
NM_020732.3:c.4591C>T	NP_065783.3:p.Pro1531Ser
XM_005267069.3:c.4711C>T	XP_005267126.2:p.Pro1571Ser
XM_011535984.1:c.3790C>T	XP_011534286.1:p.Pro1264Ser
XM_011535985.1:c.3610C>T	XP_011534287.1:p.Pro1204Ser
XM_011535986.1:c.3370C>T	XP_011534288.1:p.Pro1124Ser
XM_011535987.1:c.2989C>T	XP_011534289.1:p.Pro997Ser
XM_011535988.1:c.1852C>T	XP_011534290.1:p.Pro618Ser
NM_001346813.1:c.4711C>T	NP_001333742.1:p.Pro1571Ser
NM_001363725.1:c.2461C>T	NP_001350654.1:p.Pro821Ser
XM_011535984.2:c.4921C>T	XP_011534286.2:p.Pro1641Ser
XM_011535988.3:c.1852C>T	XP_011534290.1:p.Pro618Ser
XM_017011103.2:c.4822C>T	XP_016866592.1:p.Pro1608Ser
XM_017011104.1:c.4792C>T	XP_016866593.1:p.Pro1598Ser
XM_017011105.2:c.4762C>T	XP_016866594.1:p.Pro1588Ser
XM_017011106.2:c.4633C>T	XP_016866595.1:p.Pro1545Ser
XM_017011107.2:c.4612C>T	XP_016866596.1:p.Pro1538Ser
XR_002956289.1:n.4907C>T
NM_001363725.2:c.2461C>T	NP_001350654.1:p.Pro821Ser
NM_001371656.1:c.4840C>T	NP_001358585.1:p.Pro1614Ser
NM_001374820.1:c.4840C>T	NP_001361749.1:p.Pro1614Ser
NM_001374828.1:c.4960C>T MANE Select	NP_001361757.1:p.Pro1654Ser
NM_017519.3:c.4801C>T	NP_059989.3:p.Pro1601Ser