Canonical Allele Identifier: CA366242237

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375216
• MyVariant Identifiers: chr6:g.157522339G>C (hg19) ; chr6:g.157201205G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201205G>C , CM000668.2:g.157201205G>C	GRCh38
NC_000006.11:g.157522339G>C , CM000668.1:g.157522339G>C	GRCh37
NC_000006.10:g.157564031G>C	NCBI36
NG_032093.1:g.428276G>C
NG_032093.2:g.428276G>C
NG_066624.1:g.430180G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4821G>C	ENSP00000055163.8:p.Gln1607His
ENST00000414678.8:c.4890G>C	ENSP00000412835.3:p.Gln1630His
ENST00000637015.2:c.5109G>C	ENSP00000489729.2:p.Gln1703His
ENST00000346085.10:c.4860G>C	ENSP00000344546.5:p.Gln1620His
ENST00000350026.10:c.4572G>C	ENSP00000055163.7:p.Gln1524His
ENST00000414678.7:c.3138G>C	ENSP00000412835.2:p.Gln1046His
ENST00000635849.1:c.2301G>C	ENSP00000490948.1:p.Gln767His
ENST00000635957.1:c.1932G>C	ENSP00000490385.1:p.Gln644His
ENST00000636227.1:n.3443G>C
ENST00000636254.1:n.900G>C
ENST00000636930.2:c.4980G>C MANE Select	ENSP00000490491.2:p.Gln1660His
ENST00000636940.1:n.2977G>C
ENST00000637015.1:c.2348G>C
ENST00000637568.1:c.2262G>C
ENST00000637741.1:n.1646G>C
ENST00000637810.1:c.2322G>C	ENSP00000489636.1:p.Gln774His
ENST00000637904.1:c.2481G>C	ENSP00000490550.1:p.Gln827His
ENST00000647938.1:c.4611G>C	ENSP00000498155.1:p.Gln1537His
ENST00000346085.9:c.4611G>C	ENSP00000344546.4:p.Gln1537His
ENST00000350026.9:c.4572G>C	ENSP00000055163.7:p.Gln1524His
ENST00000414678.6:c.3138G>C	ENSP00000412835.2:p.Gln1046His
NM_017519.2:c.4572G>C	NP_059989.2:p.Gln1524His
NM_020732.3:c.4611G>C	NP_065783.3:p.Gln1537His
XM_005267069.3:c.4731G>C	XP_005267126.2:p.Gln1577His
XM_011535984.1:c.3810G>C	XP_011534286.1:p.Gln1270His
XM_011535985.1:c.3630G>C	XP_011534287.1:p.Gln1210His
XM_011535986.1:c.3390G>C	XP_011534288.1:p.Gln1130His
XM_011535987.1:c.3009G>C	XP_011534289.1:p.Gln1003His
XM_011535988.1:c.1872G>C	XP_011534290.1:p.Gln624His
NM_001346813.1:c.4731G>C	NP_001333742.1:p.Gln1577His
NM_001363725.1:c.2481G>C	NP_001350654.1:p.Gln827His
XM_011535984.2:c.4941G>C	XP_011534286.2:p.Gln1647His
XM_011535988.3:c.1872G>C	XP_011534290.1:p.Gln624His
XM_017011103.2:c.4842G>C	XP_016866592.1:p.Gln1614His
XM_017011104.1:c.4812G>C	XP_016866593.1:p.Gln1604His
XM_017011105.2:c.4782G>C	XP_016866594.1:p.Gln1594His
XM_017011106.2:c.4653G>C	XP_016866595.1:p.Gln1551His
XM_017011107.2:c.4632G>C	XP_016866596.1:p.Gln1544His
XR_002956289.1:n.4927G>C
NM_001363725.2:c.2481G>C	NP_001350654.1:p.Gln827His
NM_001371656.1:c.4860G>C	NP_001358585.1:p.Gln1620His
NM_001374820.1:c.4860G>C	NP_001361749.1:p.Gln1620His
NM_001374828.1:c.4980G>C MANE Select	NP_001361757.1:p.Gln1660His
NM_017519.3:c.4821G>C	NP_059989.3:p.Gln1607His