Canonical Allele Identifier: CA366241445

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522139A>C (hg19) ; chr6:g.157201005A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201005A>C , CM000668.2:g.157201005A>C	GRCh38
NC_000006.11:g.157522139A>C , CM000668.1:g.157522139A>C	GRCh37
NC_000006.10:g.157563831A>C	NCBI36
NG_032093.1:g.428076A>C
NG_032093.2:g.428076A>C
NG_066624.1:g.429980A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4621A>C	ENSP00000055163.8:p.Met1541Leu
ENST00000414678.8:c.4690A>C	ENSP00000412835.3:p.Met1564Leu
ENST00000637015.2:c.4909A>C	ENSP00000489729.2:p.Met1637Leu
ENST00000346085.10:c.4660A>C	ENSP00000344546.5:p.Met1554Leu
ENST00000350026.10:c.4372A>C	ENSP00000055163.7:p.Met1458Leu
ENST00000414678.7:c.2938A>C	ENSP00000412835.2:p.Met980Leu
ENST00000635849.1:c.2101A>C	ENSP00000490948.1:p.Met701Leu
ENST00000635957.1:c.1732A>C	ENSP00000490385.1:p.Met578Leu
ENST00000636227.1:n.3243A>C
ENST00000636254.1:n.700A>C
ENST00000636930.2:c.4780A>C MANE Select	ENSP00000490491.2:p.Met1594Leu
ENST00000636940.1:n.2777A>C
ENST00000637015.1:c.2148A>C
ENST00000637568.1:c.2062A>C
ENST00000637741.1:n.1446A>C
ENST00000637810.1:c.2122A>C	ENSP00000489636.1:p.Met708Leu
ENST00000637904.1:c.2281A>C	ENSP00000490550.1:p.Met761Leu
ENST00000647938.1:c.4411A>C	ENSP00000498155.1:p.Met1471Leu
ENST00000346085.9:c.4411A>C	ENSP00000344546.4:p.Met1471Leu
ENST00000350026.9:c.4372A>C	ENSP00000055163.7:p.Met1458Leu
ENST00000414678.6:c.2938A>C	ENSP00000412835.2:p.Met980Leu
NM_017519.2:c.4372A>C	NP_059989.2:p.Met1458Leu
NM_020732.3:c.4411A>C	NP_065783.3:p.Met1471Leu
XM_005267069.3:c.4531A>C	XP_005267126.2:p.Met1511Leu
XM_011535984.1:c.3610A>C	XP_011534286.1:p.Met1204Leu
XM_011535985.1:c.3430A>C	XP_011534287.1:p.Met1144Leu
XM_011535986.1:c.3190A>C	XP_011534288.1:p.Met1064Leu
XM_011535987.1:c.2809A>C	XP_011534289.1:p.Met937Leu
XM_011535988.1:c.1672A>C	XP_011534290.1:p.Met558Leu
NM_001346813.1:c.4531A>C	NP_001333742.1:p.Met1511Leu
NM_001363725.1:c.2281A>C	NP_001350654.1:p.Met761Leu
XM_011535984.2:c.4741A>C	XP_011534286.2:p.Met1581Leu
XM_011535988.3:c.1672A>C	XP_011534290.1:p.Met558Leu
XM_017011103.2:c.4642A>C	XP_016866592.1:p.Met1548Leu
XM_017011104.1:c.4612A>C	XP_016866593.1:p.Met1538Leu
XM_017011105.2:c.4582A>C	XP_016866594.1:p.Met1528Leu
XM_017011106.2:c.4453A>C	XP_016866595.1:p.Met1485Leu
XM_017011107.2:c.4432A>C	XP_016866596.1:p.Met1478Leu
XR_002956289.1:n.4727A>C
NM_001363725.2:c.2281A>C	NP_001350654.1:p.Met761Leu
NM_001371656.1:c.4660A>C	NP_001358585.1:p.Met1554Leu
NM_001374820.1:c.4660A>C	NP_001361749.1:p.Met1554Leu
NM_001374828.1:c.4780A>C MANE Select	NP_001361757.1:p.Met1594Leu
NM_017519.3:c.4621A>C	NP_059989.3:p.Met1541Leu