Canonical Allele Identifier: CA366241954

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522227T>C (hg19) ; chr6:g.157201093T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201093T>C , CM000668.2:g.157201093T>C	GRCh38
NC_000006.11:g.157522227T>C , CM000668.1:g.157522227T>C	GRCh37
NC_000006.10:g.157563919T>C	NCBI36
NG_032093.1:g.428164T>C
NG_032093.2:g.428164T>C
NG_066624.1:g.430068T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4709T>C	ENSP00000055163.8:p.Met1570Thr
ENST00000414678.8:c.4778T>C	ENSP00000412835.3:p.Met1593Thr
ENST00000637015.2:c.4997T>C	ENSP00000489729.2:p.Met1666Thr
ENST00000346085.10:c.4748T>C	ENSP00000344546.5:p.Met1583Thr
ENST00000350026.10:c.4460T>C	ENSP00000055163.7:p.Met1487Thr
ENST00000414678.7:c.3026T>C	ENSP00000412835.2:p.Met1009Thr
ENST00000635849.1:c.2189T>C	ENSP00000490948.1:p.Met730Thr
ENST00000635957.1:c.1820T>C	ENSP00000490385.1:p.Met607Thr
ENST00000636227.1:n.3331T>C
ENST00000636254.1:n.788T>C
ENST00000636930.2:c.4868T>C MANE Select	ENSP00000490491.2:p.Met1623Thr
ENST00000636940.1:n.2865T>C
ENST00000637015.1:c.2236T>C
ENST00000637568.1:c.2150T>C
ENST00000637741.1:n.1534T>C
ENST00000637810.1:c.2210T>C	ENSP00000489636.1:p.Met737Thr
ENST00000637904.1:c.2369T>C	ENSP00000490550.1:p.Met790Thr
ENST00000647938.1:c.4499T>C	ENSP00000498155.1:p.Met1500Thr
ENST00000346085.9:c.4499T>C	ENSP00000344546.4:p.Met1500Thr
ENST00000350026.9:c.4460T>C	ENSP00000055163.7:p.Met1487Thr
ENST00000414678.6:c.3026T>C	ENSP00000412835.2:p.Met1009Thr
NM_017519.2:c.4460T>C	NP_059989.2:p.Met1487Thr
NM_020732.3:c.4499T>C	NP_065783.3:p.Met1500Thr
XM_005267069.3:c.4619T>C	XP_005267126.2:p.Met1540Thr
XM_011535984.1:c.3698T>C	XP_011534286.1:p.Met1233Thr
XM_011535985.1:c.3518T>C	XP_011534287.1:p.Met1173Thr
XM_011535986.1:c.3278T>C	XP_011534288.1:p.Met1093Thr
XM_011535987.1:c.2897T>C	XP_011534289.1:p.Met966Thr
XM_011535988.1:c.1760T>C	XP_011534290.1:p.Met587Thr
NM_001346813.1:c.4619T>C	NP_001333742.1:p.Met1540Thr
NM_001363725.1:c.2369T>C	NP_001350654.1:p.Met790Thr
XM_011535984.2:c.4829T>C	XP_011534286.2:p.Met1610Thr
XM_011535988.3:c.1760T>C	XP_011534290.1:p.Met587Thr
XM_017011103.2:c.4730T>C	XP_016866592.1:p.Met1577Thr
XM_017011104.1:c.4700T>C	XP_016866593.1:p.Met1567Thr
XM_017011105.2:c.4670T>C	XP_016866594.1:p.Met1557Thr
XM_017011106.2:c.4541T>C	XP_016866595.1:p.Met1514Thr
XM_017011107.2:c.4520T>C	XP_016866596.1:p.Met1507Thr
XR_002956289.1:n.4815T>C
NM_001363725.2:c.2369T>C	NP_001350654.1:p.Met790Thr
NM_001371656.1:c.4748T>C	NP_001358585.1:p.Met1583Thr
NM_001374820.1:c.4748T>C	NP_001361749.1:p.Met1583Thr
NM_001374828.1:c.4868T>C MANE Select	NP_001361757.1:p.Met1623Thr
NM_017519.3:c.4709T>C	NP_059989.3:p.Met1570Thr