Canonical Allele Identifier: CA366241370

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157200985-T-C
• MyVariant Identifiers: chr6:g.157522119T>C (hg19) ; chr6:g.157200985T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200985T>C , CM000668.2:g.157200985T>C	GRCh38
NC_000006.11:g.157522119T>C , CM000668.1:g.157522119T>C	GRCh37
NC_000006.10:g.157563811T>C	NCBI36
NG_032093.1:g.428056T>C
NG_032093.2:g.428056T>C
NG_066624.1:g.429960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4601T>C	ENSP00000055163.8:p.Met1534Thr
ENST00000414678.8:c.4670T>C	ENSP00000412835.3:p.Met1557Thr
ENST00000637015.2:c.4889T>C	ENSP00000489729.2:p.Met1630Thr
ENST00000346085.10:c.4640T>C	ENSP00000344546.5:p.Met1547Thr
ENST00000350026.10:c.4352T>C	ENSP00000055163.7:p.Met1451Thr
ENST00000414678.7:c.2918T>C	ENSP00000412835.2:p.Met973Thr
ENST00000635849.1:c.2081T>C	ENSP00000490948.1:p.Met694Thr
ENST00000635957.1:c.1712T>C	ENSP00000490385.1:p.Met571Thr
ENST00000636227.1:n.3223T>C
ENST00000636254.1:n.680T>C
ENST00000636930.2:c.4760T>C MANE Select	ENSP00000490491.2:p.Met1587Thr
ENST00000636940.1:n.2757T>C
ENST00000637015.1:c.2128T>C
ENST00000637568.1:c.2042T>C
ENST00000637741.1:n.1426T>C
ENST00000637810.1:c.2102T>C	ENSP00000489636.1:p.Met701Thr
ENST00000637904.1:c.2261T>C	ENSP00000490550.1:p.Met754Thr
ENST00000647938.1:c.4391T>C	ENSP00000498155.1:p.Met1464Thr
ENST00000346085.9:c.4391T>C	ENSP00000344546.4:p.Met1464Thr
ENST00000350026.9:c.4352T>C	ENSP00000055163.7:p.Met1451Thr
ENST00000414678.6:c.2918T>C	ENSP00000412835.2:p.Met973Thr
NM_017519.2:c.4352T>C	NP_059989.2:p.Met1451Thr
NM_020732.3:c.4391T>C	NP_065783.3:p.Met1464Thr
XM_005267069.3:c.4511T>C	XP_005267126.2:p.Met1504Thr
XM_011535984.1:c.3590T>C	XP_011534286.1:p.Met1197Thr
XM_011535985.1:c.3410T>C	XP_011534287.1:p.Met1137Thr
XM_011535986.1:c.3170T>C	XP_011534288.1:p.Met1057Thr
XM_011535987.1:c.2789T>C	XP_011534289.1:p.Met930Thr
XM_011535988.1:c.1652T>C	XP_011534290.1:p.Met551Thr
NM_001346813.1:c.4511T>C	NP_001333742.1:p.Met1504Thr
NM_001363725.1:c.2261T>C	NP_001350654.1:p.Met754Thr
XM_011535984.2:c.4721T>C	XP_011534286.2:p.Met1574Thr
XM_011535988.3:c.1652T>C	XP_011534290.1:p.Met551Thr
XM_017011103.2:c.4622T>C	XP_016866592.1:p.Met1541Thr
XM_017011104.1:c.4592T>C	XP_016866593.1:p.Met1531Thr
XM_017011105.2:c.4562T>C	XP_016866594.1:p.Met1521Thr
XM_017011106.2:c.4433T>C	XP_016866595.1:p.Met1478Thr
XM_017011107.2:c.4412T>C	XP_016866596.1:p.Met1471Thr
XR_002956289.1:n.4707T>C
NM_001363725.2:c.2261T>C	NP_001350654.1:p.Met754Thr
NM_001371656.1:c.4640T>C	NP_001358585.1:p.Met1547Thr
NM_001374820.1:c.4640T>C	NP_001361749.1:p.Met1547Thr
NM_001374828.1:c.4760T>C MANE Select	NP_001361757.1:p.Met1587Thr
NM_017519.3:c.4601T>C	NP_059989.3:p.Met1534Thr