Canonical Allele Identifier: CA366241670

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522176G>C (hg19) ; chr6:g.157201042G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201042G>C , CM000668.2:g.157201042G>C	GRCh38
NC_000006.11:g.157522176G>C , CM000668.1:g.157522176G>C	GRCh37
NC_000006.10:g.157563868G>C	NCBI36
NG_032093.1:g.428113G>C
NG_032093.2:g.428113G>C
NG_066624.1:g.430017G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4658G>C	ENSP00000055163.8:p.Gly1553Ala
ENST00000414678.8:c.4727G>C	ENSP00000412835.3:p.Gly1576Ala
ENST00000637015.2:c.4946G>C	ENSP00000489729.2:p.Gly1649Ala
ENST00000346085.10:c.4697G>C	ENSP00000344546.5:p.Gly1566Ala
ENST00000350026.10:c.4409G>C	ENSP00000055163.7:p.Gly1470Ala
ENST00000414678.7:c.2975G>C	ENSP00000412835.2:p.Gly992Ala
ENST00000635849.1:c.2138G>C	ENSP00000490948.1:p.Gly713Ala
ENST00000635957.1:c.1769G>C	ENSP00000490385.1:p.Gly590Ala
ENST00000636227.1:n.3280G>C
ENST00000636254.1:n.737G>C
ENST00000636930.2:c.4817G>C MANE Select	ENSP00000490491.2:p.Gly1606Ala
ENST00000636940.1:n.2814G>C
ENST00000637015.1:c.2185G>C
ENST00000637568.1:c.2099G>C
ENST00000637741.1:n.1483G>C
ENST00000637810.1:c.2159G>C	ENSP00000489636.1:p.Gly720Ala
ENST00000637904.1:c.2318G>C	ENSP00000490550.1:p.Gly773Ala
ENST00000647938.1:c.4448G>C	ENSP00000498155.1:p.Gly1483Ala
ENST00000346085.9:c.4448G>C	ENSP00000344546.4:p.Gly1483Ala
ENST00000350026.9:c.4409G>C	ENSP00000055163.7:p.Gly1470Ala
ENST00000414678.6:c.2975G>C	ENSP00000412835.2:p.Gly992Ala
NM_017519.2:c.4409G>C	NP_059989.2:p.Gly1470Ala
NM_020732.3:c.4448G>C	NP_065783.3:p.Gly1483Ala
XM_005267069.3:c.4568G>C	XP_005267126.2:p.Gly1523Ala
XM_011535984.1:c.3647G>C	XP_011534286.1:p.Gly1216Ala
XM_011535985.1:c.3467G>C	XP_011534287.1:p.Gly1156Ala
XM_011535986.1:c.3227G>C	XP_011534288.1:p.Gly1076Ala
XM_011535987.1:c.2846G>C	XP_011534289.1:p.Gly949Ala
XM_011535988.1:c.1709G>C	XP_011534290.1:p.Gly570Ala
NM_001346813.1:c.4568G>C	NP_001333742.1:p.Gly1523Ala
NM_001363725.1:c.2318G>C	NP_001350654.1:p.Gly773Ala
XM_011535984.2:c.4778G>C	XP_011534286.2:p.Gly1593Ala
XM_011535988.3:c.1709G>C	XP_011534290.1:p.Gly570Ala
XM_017011103.2:c.4679G>C	XP_016866592.1:p.Gly1560Ala
XM_017011104.1:c.4649G>C	XP_016866593.1:p.Gly1550Ala
XM_017011105.2:c.4619G>C	XP_016866594.1:p.Gly1540Ala
XM_017011106.2:c.4490G>C	XP_016866595.1:p.Gly1497Ala
XM_017011107.2:c.4469G>C	XP_016866596.1:p.Gly1490Ala
XR_002956289.1:n.4764G>C
NM_001363725.2:c.2318G>C	NP_001350654.1:p.Gly773Ala
NM_001371656.1:c.4697G>C	NP_001358585.1:p.Gly1566Ala
NM_001374820.1:c.4697G>C	NP_001361749.1:p.Gly1566Ala
NM_001374828.1:c.4817G>C MANE Select	NP_001361757.1:p.Gly1606Ala
NM_017519.3:c.4658G>C	NP_059989.3:p.Gly1553Ala