Canonical Allele Identifier: CA366242101

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374852
• gnomAD v4: 6-157201144-G-C
• MyVariant Identifiers: chr6:g.157522278G>C (hg19) ; chr6:g.157201144G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201144G>C , CM000668.2:g.157201144G>C	GRCh38
NC_000006.11:g.157522278G>C , CM000668.1:g.157522278G>C	GRCh37
NC_000006.10:g.157563970G>C	NCBI36
NG_032093.1:g.428215G>C
NG_032093.2:g.428215G>C
NG_066624.1:g.430119G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4760G>C	ENSP00000055163.8:p.Ser1587Thr
ENST00000414678.8:c.4829G>C	ENSP00000412835.3:p.Ser1610Thr
ENST00000637015.2:c.5048G>C	ENSP00000489729.2:p.Ser1683Thr
ENST00000346085.10:c.4799G>C	ENSP00000344546.5:p.Ser1600Thr
ENST00000350026.10:c.4511G>C	ENSP00000055163.7:p.Ser1504Thr
ENST00000414678.7:c.3077G>C	ENSP00000412835.2:p.Ser1026Thr
ENST00000635849.1:c.2240G>C	ENSP00000490948.1:p.Ser747Thr
ENST00000635957.1:c.1871G>C	ENSP00000490385.1:p.Ser624Thr
ENST00000636227.1:n.3382G>C
ENST00000636254.1:n.839G>C
ENST00000636930.2:c.4919G>C MANE Select	ENSP00000490491.2:p.Ser1640Thr
ENST00000636940.1:n.2916G>C
ENST00000637015.1:c.2287G>C
ENST00000637568.1:c.2201G>C
ENST00000637741.1:n.1585G>C
ENST00000637810.1:c.2261G>C	ENSP00000489636.1:p.Ser754Thr
ENST00000637904.1:c.2420G>C	ENSP00000490550.1:p.Ser807Thr
ENST00000647938.1:c.4550G>C	ENSP00000498155.1:p.Ser1517Thr
ENST00000346085.9:c.4550G>C	ENSP00000344546.4:p.Ser1517Thr
ENST00000350026.9:c.4511G>C	ENSP00000055163.7:p.Ser1504Thr
ENST00000414678.6:c.3077G>C	ENSP00000412835.2:p.Ser1026Thr
NM_017519.2:c.4511G>C	NP_059989.2:p.Ser1504Thr
NM_020732.3:c.4550G>C	NP_065783.3:p.Ser1517Thr
XM_005267069.3:c.4670G>C	XP_005267126.2:p.Ser1557Thr
XM_011535984.1:c.3749G>C	XP_011534286.1:p.Ser1250Thr
XM_011535985.1:c.3569G>C	XP_011534287.1:p.Ser1190Thr
XM_011535986.1:c.3329G>C	XP_011534288.1:p.Ser1110Thr
XM_011535987.1:c.2948G>C	XP_011534289.1:p.Ser983Thr
XM_011535988.1:c.1811G>C	XP_011534290.1:p.Ser604Thr
NM_001346813.1:c.4670G>C	NP_001333742.1:p.Ser1557Thr
NM_001363725.1:c.2420G>C	NP_001350654.1:p.Ser807Thr
XM_011535984.2:c.4880G>C	XP_011534286.2:p.Ser1627Thr
XM_011535988.3:c.1811G>C	XP_011534290.1:p.Ser604Thr
XM_017011103.2:c.4781G>C	XP_016866592.1:p.Ser1594Thr
XM_017011104.1:c.4751G>C	XP_016866593.1:p.Ser1584Thr
XM_017011105.2:c.4721G>C	XP_016866594.1:p.Ser1574Thr
XM_017011106.2:c.4592G>C	XP_016866595.1:p.Ser1531Thr
XM_017011107.2:c.4571G>C	XP_016866596.1:p.Ser1524Thr
XR_002956289.1:n.4866G>C
NM_001363725.2:c.2420G>C	NP_001350654.1:p.Ser807Thr
NM_001371656.1:c.4799G>C	NP_001358585.1:p.Ser1600Thr
NM_001374820.1:c.4799G>C	NP_001361749.1:p.Ser1600Thr
NM_001374828.1:c.4919G>C MANE Select	NP_001361757.1:p.Ser1640Thr
NM_017519.3:c.4760G>C	NP_059989.3:p.Ser1587Thr