Canonical Allele Identifier: CA366241375

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157200986-G-T
• MyVariant Identifiers: chr6:g.157522120G>T (hg19) ; chr6:g.157200986G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200986G>T , CM000668.2:g.157200986G>T	GRCh38
NC_000006.11:g.157522120G>T , CM000668.1:g.157522120G>T	GRCh37
NC_000006.10:g.157563812G>T	NCBI36
NG_032093.1:g.428057G>T
NG_032093.2:g.428057G>T
NG_066624.1:g.429961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4602G>T	ENSP00000055163.8:p.Met1534Ile
ENST00000414678.8:c.4671G>T	ENSP00000412835.3:p.Met1557Ile
ENST00000637015.2:c.4890G>T	ENSP00000489729.2:p.Met1630Ile
ENST00000346085.10:c.4641G>T	ENSP00000344546.5:p.Met1547Ile
ENST00000350026.10:c.4353G>T	ENSP00000055163.7:p.Met1451Ile
ENST00000414678.7:c.2919G>T	ENSP00000412835.2:p.Met973Ile
ENST00000635849.1:c.2082G>T	ENSP00000490948.1:p.Met694Ile
ENST00000635957.1:c.1713G>T	ENSP00000490385.1:p.Met571Ile
ENST00000636227.1:n.3224G>T
ENST00000636254.1:n.681G>T
ENST00000636930.2:c.4761G>T MANE Select	ENSP00000490491.2:p.Met1587Ile
ENST00000636940.1:n.2758G>T
ENST00000637015.1:c.2129G>T
ENST00000637568.1:c.2043G>T
ENST00000637741.1:n.1427G>T
ENST00000637810.1:c.2103G>T	ENSP00000489636.1:p.Met701Ile
ENST00000637904.1:c.2262G>T	ENSP00000490550.1:p.Met754Ile
ENST00000647938.1:c.4392G>T	ENSP00000498155.1:p.Met1464Ile
ENST00000346085.9:c.4392G>T	ENSP00000344546.4:p.Met1464Ile
ENST00000350026.9:c.4353G>T	ENSP00000055163.7:p.Met1451Ile
ENST00000414678.6:c.2919G>T	ENSP00000412835.2:p.Met973Ile
NM_017519.2:c.4353G>T	NP_059989.2:p.Met1451Ile
NM_020732.3:c.4392G>T	NP_065783.3:p.Met1464Ile
XM_005267069.3:c.4512G>T	XP_005267126.2:p.Met1504Ile
XM_011535984.1:c.3591G>T	XP_011534286.1:p.Met1197Ile
XM_011535985.1:c.3411G>T	XP_011534287.1:p.Met1137Ile
XM_011535986.1:c.3171G>T	XP_011534288.1:p.Met1057Ile
XM_011535987.1:c.2790G>T	XP_011534289.1:p.Met930Ile
XM_011535988.1:c.1653G>T	XP_011534290.1:p.Met551Ile
NM_001346813.1:c.4512G>T	NP_001333742.1:p.Met1504Ile
NM_001363725.1:c.2262G>T	NP_001350654.1:p.Met754Ile
XM_011535984.2:c.4722G>T	XP_011534286.2:p.Met1574Ile
XM_011535988.3:c.1653G>T	XP_011534290.1:p.Met551Ile
XM_017011103.2:c.4623G>T	XP_016866592.1:p.Met1541Ile
XM_017011104.1:c.4593G>T	XP_016866593.1:p.Met1531Ile
XM_017011105.2:c.4563G>T	XP_016866594.1:p.Met1521Ile
XM_017011106.2:c.4434G>T	XP_016866595.1:p.Met1478Ile
XM_017011107.2:c.4413G>T	XP_016866596.1:p.Met1471Ile
XR_002956289.1:n.4708G>T
NM_001363725.2:c.2262G>T	NP_001350654.1:p.Met754Ile
NM_001371656.1:c.4641G>T	NP_001358585.1:p.Met1547Ile
NM_001374820.1:c.4641G>T	NP_001361749.1:p.Met1547Ile
NM_001374828.1:c.4761G>T MANE Select	NP_001361757.1:p.Met1587Ile
NM_017519.3:c.4602G>T	NP_059989.3:p.Met1534Ile