Canonical Allele Identifier: CA366389253

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2663855
• ClinVar RCV Id: RCV003444085
• dbSNP Id: rs1554226145
• MyVariant Identifiers: chr6:g.157470057C>T (hg19) ; chr6:g.157148923C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148923C>T , CM000668.2:g.157148923C>T	GRCh38
NC_000006.11:g.157470057C>T , CM000668.1:g.157470057C>T	GRCh37
NC_000006.10:g.157511749C>T	NCBI36
NG_032093.1:g.375994C>T
NG_032093.2:g.375994C>T
NG_066624.1:g.377898C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3061C>T	ENSP00000055163.8:p.Gln1021Ter
ENST00000414678.8:c.2971C>T	ENSP00000412835.3:p.Gln991Ter
ENST00000637015.2:c.3061C>T	ENSP00000489729.2:p.Gln1021Ter
ENST00000319584.11:c.1075C>T	ENSP00000313006.7:p.Gln359Ter
ENST00000346085.10:c.3100C>T	ENSP00000344546.5:p.Gln1034Ter
ENST00000350026.10:c.2812C>T	ENSP00000055163.7:p.Gln938Ter
ENST00000414678.7:c.1219C>T	ENSP00000412835.2:p.Gln407Ter
ENST00000452544.2:n.962C>T
ENST00000635849.1:c.382C>T	ENSP00000490948.1:p.Gln128Ter
ENST00000635957.1:c.16C>T	ENSP00000490385.1:p.Gln6Ter
ENST00000636426.1:n.195C>T
ENST00000636930.2:c.3061C>T MANE Select	ENSP00000490491.2:p.Gln1021Ter
ENST00000637015.1:c.300C>T
ENST00000637568.1:c.104C>T
ENST00000637810.1:c.562C>T	ENSP00000489636.1:p.Gln188Ter
ENST00000637904.1:c.562C>T	ENSP00000490550.1:p.Gln188Ter
ENST00000647938.1:c.2851C>T	ENSP00000498155.1:p.Gln951Ter
ENST00000674190.1:n.1810C>T
ENST00000319584.10:c.1078C>T	ENSP00000313006.6:p.Gln360Ter
ENST00000346085.9:c.2851C>T	ENSP00000344546.4:p.Gln951Ter
ENST00000350026.9:c.2812C>T	ENSP00000055163.7:p.Gln938Ter
ENST00000400790.3:c.13C>T	ENSP00000383596.3:p.Gln5Ter
ENST00000414678.6:c.1219C>T	ENSP00000412835.2:p.Gln407Ter
ENST00000452544.1:n.908C>T
ENST00000478761.3:c.134C>T
NM_017519.2:c.2812C>T	NP_059989.2:p.Gln938Ter
NM_020732.3:c.2851C>T	NP_065783.3:p.Gln951Ter
XM_005267069.3:c.2812C>T	XP_005267126.2:p.Gln938Ter
XM_011535984.1:c.1762C>T	XP_011534286.1:p.Gln588Ter
XM_011535985.1:c.1582C>T	XP_011534287.1:p.Gln528Ter
XM_011535986.1:c.1342C>T	XP_011534288.1:p.Gln448Ter
XM_011535987.1:c.961C>T	XP_011534289.1:p.Gln321Ter
XM_011535988.1:c.-20+15716C>T	XP_011534290.1:n.-20+15716C>T
NM_001346813.1:c.2812C>T	NP_001333742.1:p.Gln938Ter
NM_001363725.1:c.562C>T	NP_001350654.1:p.Gln188Ter
XM_011535984.2:c.2893C>T	XP_011534286.2:p.Gln965Ter
XM_011535988.3:c.-20+15716C>T	XP_011534290.1:n.-20+15716C>T
XM_017011103.2:c.2893C>T	XP_016866592.1:p.Gln965Ter
XM_017011104.1:c.2893C>T	XP_016866593.1:p.Gln965Ter
XM_017011105.2:c.2893C>T	XP_016866594.1:p.Gln965Ter
XM_017011106.2:c.2893C>T	XP_016866595.1:p.Gln965Ter
XM_017011107.2:c.2713C>T	XP_016866596.1:p.Gln905Ter
XR_002956289.1:n.2976C>T
NM_001363725.2:c.562C>T	NP_001350654.1:p.Gln188Ter
NM_001371656.1:c.3100C>T	NP_001358585.1:p.Gln1034Ter
NM_001374820.1:c.3100C>T	NP_001361749.1:p.Gln1034Ter
NM_001374828.1:c.3061C>T MANE Select	NP_001361757.1:p.Gln1021Ter
NM_017519.3:c.3061C>T	NP_059989.3:p.Gln1021Ter