Canonical Allele Identifier: CA366240904

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521910G>C (hg19) ; chr6:g.157200776G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200776G>C , CM000668.2:g.157200776G>C	GRCh38
NC_000006.11:g.157521910G>C , CM000668.1:g.157521910G>C	GRCh37
NC_000006.10:g.157563602G>C	NCBI36
NG_032093.1:g.427847G>C
NG_032093.2:g.427847G>C
NG_066624.1:g.429751G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4392G>C	ENSP00000055163.8:p.Met1464Ile
ENST00000414678.8:c.4461G>C	ENSP00000412835.3:p.Met1487Ile
ENST00000637015.2:c.4680G>C	ENSP00000489729.2:p.Met1560Ile
ENST00000346085.10:c.4431G>C	ENSP00000344546.5:p.Met1477Ile
ENST00000350026.10:c.4143G>C	ENSP00000055163.7:p.Met1381Ile
ENST00000414678.7:c.2709G>C	ENSP00000412835.2:p.Met903Ile
ENST00000635849.1:c.1872G>C	ENSP00000490948.1:p.Met624Ile
ENST00000635957.1:c.1503G>C	ENSP00000490385.1:p.Met501Ile
ENST00000636227.1:n.3014G>C
ENST00000636254.1:n.471G>C
ENST00000636930.2:c.4551G>C MANE Select	ENSP00000490491.2:p.Met1517Ile
ENST00000636940.1:n.2548G>C
ENST00000637015.1:c.1919G>C
ENST00000637568.1:c.1833G>C
ENST00000637741.1:n.1217G>C
ENST00000637810.1:c.1893G>C	ENSP00000489636.1:p.Met631Ile
ENST00000637904.1:c.2052G>C	ENSP00000490550.1:p.Met684Ile
ENST00000647938.1:c.4182G>C	ENSP00000498155.1:p.Met1394Ile
ENST00000346085.9:c.4182G>C	ENSP00000344546.4:p.Met1394Ile
ENST00000350026.9:c.4143G>C	ENSP00000055163.7:p.Met1381Ile
ENST00000414678.6:c.2709G>C	ENSP00000412835.2:p.Met903Ile
NM_017519.2:c.4143G>C	NP_059989.2:p.Met1381Ile
NM_020732.3:c.4182G>C	NP_065783.3:p.Met1394Ile
XM_005267069.3:c.4302G>C	XP_005267126.2:p.Met1434Ile
XM_011535984.1:c.3381G>C	XP_011534286.1:p.Met1127Ile
XM_011535985.1:c.3201G>C	XP_011534287.1:p.Met1067Ile
XM_011535986.1:c.2961G>C	XP_011534288.1:p.Met987Ile
XM_011535987.1:c.2580G>C	XP_011534289.1:p.Met860Ile
XM_011535988.1:c.1443G>C	XP_011534290.1:p.Met481Ile
NM_001346813.1:c.4302G>C	NP_001333742.1:p.Met1434Ile
NM_001363725.1:c.2052G>C	NP_001350654.1:p.Met684Ile
XM_011535984.2:c.4512G>C	XP_011534286.2:p.Met1504Ile
XM_011535988.3:c.1443G>C	XP_011534290.1:p.Met481Ile
XM_017011103.2:c.4413G>C	XP_016866592.1:p.Met1471Ile
XM_017011104.1:c.4383G>C	XP_016866593.1:p.Met1461Ile
XM_017011105.2:c.4353G>C	XP_016866594.1:p.Met1451Ile
XM_017011106.2:c.4224G>C	XP_016866595.1:p.Met1408Ile
XM_017011107.2:c.4203G>C	XP_016866596.1:p.Met1401Ile
XR_002956289.1:n.4498G>C
NM_001363725.2:c.2052G>C	NP_001350654.1:p.Met684Ile
NM_001371656.1:c.4431G>C	NP_001358585.1:p.Met1477Ile
NM_001374820.1:c.4431G>C	NP_001361749.1:p.Met1477Ile
NM_001374828.1:c.4551G>C MANE Select	NP_001361757.1:p.Met1517Ile
NM_017519.3:c.4392G>C	NP_059989.3:p.Met1464Ile