Canonical Allele Identifier: CA366242660

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 3129401
• ClinVar RCV Id: RCV004425267
• dbSNP Id: rs1794106775
• MyVariant Identifiers: chr6:g.157522479T>C (hg19) ; chr6:g.157201345T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201345T>C , CM000668.2:g.157201345T>C	GRCh38
NC_000006.11:g.157522479T>C , CM000668.1:g.157522479T>C	GRCh37
NC_000006.10:g.157564171T>C	NCBI36
NG_032093.1:g.428416T>C
NG_032093.2:g.428416T>C
NG_066624.1:g.430320T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4961T>C	ENSP00000055163.8:p.Met1654Thr
ENST00000414678.8:c.5030T>C	ENSP00000412835.3:p.Met1677Thr
ENST00000637015.2:c.5249T>C	ENSP00000489729.2:p.Met1750Thr
ENST00000346085.10:c.5000T>C	ENSP00000344546.5:p.Met1667Thr
ENST00000350026.10:c.4712T>C	ENSP00000055163.7:p.Met1571Thr
ENST00000414678.7:c.3278T>C	ENSP00000412835.2:p.Met1093Thr
ENST00000635849.1:c.2441T>C	ENSP00000490948.1:p.Met814Thr
ENST00000635957.1:c.2072T>C	ENSP00000490385.1:p.Met691Thr
ENST00000636227.1:n.3583T>C
ENST00000636254.1:n.1040T>C
ENST00000636930.2:c.5120T>C MANE Select	ENSP00000490491.2:p.Met1707Thr
ENST00000636940.1:n.3117T>C
ENST00000637015.1:c.2488T>C
ENST00000637568.1:c.2402T>C
ENST00000637741.1:n.1786T>C
ENST00000637810.1:c.2462T>C	ENSP00000489636.1:p.Met821Thr
ENST00000637904.1:c.2621T>C	ENSP00000490550.1:p.Met874Thr
ENST00000647938.1:c.4751T>C	ENSP00000498155.1:p.Met1584Thr
ENST00000346085.9:c.4751T>C	ENSP00000344546.4:p.Met1584Thr
ENST00000350026.9:c.4712T>C	ENSP00000055163.7:p.Met1571Thr
ENST00000414678.6:c.3278T>C	ENSP00000412835.2:p.Met1093Thr
NM_017519.2:c.4712T>C	NP_059989.2:p.Met1571Thr
NM_020732.3:c.4751T>C	NP_065783.3:p.Met1584Thr
XM_005267069.3:c.4871T>C	XP_005267126.2:p.Met1624Thr
XM_011535984.1:c.3950T>C	XP_011534286.1:p.Met1317Thr
XM_011535985.1:c.3770T>C	XP_011534287.1:p.Met1257Thr
XM_011535986.1:c.3530T>C	XP_011534288.1:p.Met1177Thr
XM_011535987.1:c.3149T>C	XP_011534289.1:p.Met1050Thr
XM_011535988.1:c.2012T>C	XP_011534290.1:p.Met671Thr
NM_001346813.1:c.4871T>C	NP_001333742.1:p.Met1624Thr
NM_001363725.1:c.2621T>C	NP_001350654.1:p.Met874Thr
XM_011535984.2:c.5081T>C	XP_011534286.2:p.Met1694Thr
XM_011535988.3:c.2012T>C	XP_011534290.1:p.Met671Thr
XM_017011103.2:c.4982T>C	XP_016866592.1:p.Met1661Thr
XM_017011104.1:c.4952T>C	XP_016866593.1:p.Met1651Thr
XM_017011105.2:c.4922T>C	XP_016866594.1:p.Met1641Thr
XM_017011106.2:c.4793T>C	XP_016866595.1:p.Met1598Thr
XM_017011107.2:c.4772T>C	XP_016866596.1:p.Met1591Thr
XR_002956289.1:n.5067T>C
NM_001363725.2:c.2621T>C	NP_001350654.1:p.Met874Thr
NM_001371656.1:c.5000T>C	NP_001358585.1:p.Met1667Thr
NM_001374820.1:c.5000T>C	NP_001361749.1:p.Met1667Thr
NM_001374828.1:c.5120T>C MANE Select	NP_001361757.1:p.Met1707Thr
NM_017519.3:c.4961T>C	NP_059989.3:p.Met1654Thr