Canonical Allele Identifier: CA366241967

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522229G>C (hg19) ; chr6:g.157201095G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201095G>C , CM000668.2:g.157201095G>C	GRCh38
NC_000006.11:g.157522229G>C , CM000668.1:g.157522229G>C	GRCh37
NC_000006.10:g.157563921G>C	NCBI36
NG_032093.1:g.428166G>C
NG_032093.2:g.428166G>C
NG_066624.1:g.430070G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4711G>C	ENSP00000055163.8:p.Val1571Leu
ENST00000414678.8:c.4780G>C	ENSP00000412835.3:p.Val1594Leu
ENST00000637015.2:c.4999G>C	ENSP00000489729.2:p.Val1667Leu
ENST00000346085.10:c.4750G>C	ENSP00000344546.5:p.Val1584Leu
ENST00000350026.10:c.4462G>C	ENSP00000055163.7:p.Val1488Leu
ENST00000414678.7:c.3028G>C	ENSP00000412835.2:p.Val1010Leu
ENST00000635849.1:c.2191G>C	ENSP00000490948.1:p.Val731Leu
ENST00000635957.1:c.1822G>C	ENSP00000490385.1:p.Val608Leu
ENST00000636227.1:n.3333G>C
ENST00000636254.1:n.790G>C
ENST00000636930.2:c.4870G>C MANE Select	ENSP00000490491.2:p.Val1624Leu
ENST00000636940.1:n.2867G>C
ENST00000637015.1:c.2238G>C
ENST00000637568.1:c.2152G>C
ENST00000637741.1:n.1536G>C
ENST00000637810.1:c.2212G>C	ENSP00000489636.1:p.Val738Leu
ENST00000637904.1:c.2371G>C	ENSP00000490550.1:p.Val791Leu
ENST00000647938.1:c.4501G>C	ENSP00000498155.1:p.Val1501Leu
ENST00000346085.9:c.4501G>C	ENSP00000344546.4:p.Val1501Leu
ENST00000350026.9:c.4462G>C	ENSP00000055163.7:p.Val1488Leu
ENST00000414678.6:c.3028G>C	ENSP00000412835.2:p.Val1010Leu
NM_017519.2:c.4462G>C	NP_059989.2:p.Val1488Leu
NM_020732.3:c.4501G>C	NP_065783.3:p.Val1501Leu
XM_005267069.3:c.4621G>C	XP_005267126.2:p.Val1541Leu
XM_011535984.1:c.3700G>C	XP_011534286.1:p.Val1234Leu
XM_011535985.1:c.3520G>C	XP_011534287.1:p.Val1174Leu
XM_011535986.1:c.3280G>C	XP_011534288.1:p.Val1094Leu
XM_011535987.1:c.2899G>C	XP_011534289.1:p.Val967Leu
XM_011535988.1:c.1762G>C	XP_011534290.1:p.Val588Leu
NM_001346813.1:c.4621G>C	NP_001333742.1:p.Val1541Leu
NM_001363725.1:c.2371G>C	NP_001350654.1:p.Val791Leu
XM_011535984.2:c.4831G>C	XP_011534286.2:p.Val1611Leu
XM_011535988.3:c.1762G>C	XP_011534290.1:p.Val588Leu
XM_017011103.2:c.4732G>C	XP_016866592.1:p.Val1578Leu
XM_017011104.1:c.4702G>C	XP_016866593.1:p.Val1568Leu
XM_017011105.2:c.4672G>C	XP_016866594.1:p.Val1558Leu
XM_017011106.2:c.4543G>C	XP_016866595.1:p.Val1515Leu
XM_017011107.2:c.4522G>C	XP_016866596.1:p.Val1508Leu
XR_002956289.1:n.4817G>C
NM_001363725.2:c.2371G>C	NP_001350654.1:p.Val791Leu
NM_001371656.1:c.4750G>C	NP_001358585.1:p.Val1584Leu
NM_001374820.1:c.4750G>C	NP_001361749.1:p.Val1584Leu
NM_001374828.1:c.4870G>C MANE Select	NP_001361757.1:p.Val1624Leu
NM_017519.3:c.4711G>C	NP_059989.3:p.Val1571Leu