Canonical Allele Identifier: CA366242588

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201333-T-C
• MyVariant Identifiers: chr6:g.157522467T>C (hg19) ; chr6:g.157201333T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201333T>C , CM000668.2:g.157201333T>C	GRCh38
NC_000006.11:g.157522467T>C , CM000668.1:g.157522467T>C	GRCh37
NC_000006.10:g.157564159T>C	NCBI36
NG_032093.1:g.428404T>C
NG_032093.2:g.428404T>C
NG_066624.1:g.430308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4949T>C	ENSP00000055163.8:p.Met1650Thr
ENST00000414678.8:c.5018T>C	ENSP00000412835.3:p.Met1673Thr
ENST00000637015.2:c.5237T>C	ENSP00000489729.2:p.Met1746Thr
ENST00000346085.10:c.4988T>C	ENSP00000344546.5:p.Met1663Thr
ENST00000350026.10:c.4700T>C	ENSP00000055163.7:p.Met1567Thr
ENST00000414678.7:c.3266T>C	ENSP00000412835.2:p.Met1089Thr
ENST00000635849.1:c.2429T>C	ENSP00000490948.1:p.Met810Thr
ENST00000635957.1:c.2060T>C	ENSP00000490385.1:p.Met687Thr
ENST00000636227.1:n.3571T>C
ENST00000636254.1:n.1028T>C
ENST00000636930.2:c.5108T>C MANE Select	ENSP00000490491.2:p.Met1703Thr
ENST00000636940.1:n.3105T>C
ENST00000637015.1:c.2476T>C
ENST00000637568.1:c.2390T>C
ENST00000637741.1:n.1774T>C
ENST00000637810.1:c.2450T>C	ENSP00000489636.1:p.Met817Thr
ENST00000637904.1:c.2609T>C	ENSP00000490550.1:p.Met870Thr
ENST00000647938.1:c.4739T>C	ENSP00000498155.1:p.Met1580Thr
ENST00000346085.9:c.4739T>C	ENSP00000344546.4:p.Met1580Thr
ENST00000350026.9:c.4700T>C	ENSP00000055163.7:p.Met1567Thr
ENST00000414678.6:c.3266T>C	ENSP00000412835.2:p.Met1089Thr
NM_017519.2:c.4700T>C	NP_059989.2:p.Met1567Thr
NM_020732.3:c.4739T>C	NP_065783.3:p.Met1580Thr
XM_005267069.3:c.4859T>C	XP_005267126.2:p.Met1620Thr
XM_011535984.1:c.3938T>C	XP_011534286.1:p.Met1313Thr
XM_011535985.1:c.3758T>C	XP_011534287.1:p.Met1253Thr
XM_011535986.1:c.3518T>C	XP_011534288.1:p.Met1173Thr
XM_011535987.1:c.3137T>C	XP_011534289.1:p.Met1046Thr
XM_011535988.1:c.2000T>C	XP_011534290.1:p.Met667Thr
NM_001346813.1:c.4859T>C	NP_001333742.1:p.Met1620Thr
NM_001363725.1:c.2609T>C	NP_001350654.1:p.Met870Thr
XM_011535984.2:c.5069T>C	XP_011534286.2:p.Met1690Thr
XM_011535988.3:c.2000T>C	XP_011534290.1:p.Met667Thr
XM_017011103.2:c.4970T>C	XP_016866592.1:p.Met1657Thr
XM_017011104.1:c.4940T>C	XP_016866593.1:p.Met1647Thr
XM_017011105.2:c.4910T>C	XP_016866594.1:p.Met1637Thr
XM_017011106.2:c.4781T>C	XP_016866595.1:p.Met1594Thr
XM_017011107.2:c.4760T>C	XP_016866596.1:p.Met1587Thr
XR_002956289.1:n.5055T>C
NM_001363725.2:c.2609T>C	NP_001350654.1:p.Met870Thr
NM_001371656.1:c.4988T>C	NP_001358585.1:p.Met1663Thr
NM_001374820.1:c.4988T>C	NP_001361749.1:p.Met1663Thr
NM_001374828.1:c.5108T>C MANE Select	NP_001361757.1:p.Met1703Thr
NM_017519.3:c.4949T>C	NP_059989.3:p.Met1650Thr