Canonical Allele Identifier: CA366230913

Gene: ARID1B

Linked Data

• dbSNP Id: rs886039699
• MyVariant Identifiers: chr6:g.157505570G>C (hg19) ; chr6:g.157184436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184436G>C , CM000668.2:g.157184436G>C	GRCh38
NC_000006.11:g.157505570G>C , CM000668.1:g.157505570G>C	GRCh37
NC_000006.10:g.157547262G>C	NCBI36
NG_032093.1:g.411507G>C
NG_032093.2:g.411507G>C
NG_066624.1:g.413411G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3760+1G>C	ENSP00000055163.8:n.3760+1G>C
ENST00000414678.8:c.3829+1G>C	ENSP00000412835.3:n.3829+1G>C
ENST00000637015.2:c.4048+1G>C	ENSP00000489729.2:n.4048+1G>C
ENST00000319584.11:c.1933+1G>C	ENSP00000313006.7:n.1933+1G>C
ENST00000346085.10:c.3799+1G>C	ENSP00000344546.5:n.3799+1G>C
ENST00000350026.10:c.3511+1G>C	ENSP00000055163.7:n.3511+1G>C
ENST00000414678.7:c.2077+1G>C	ENSP00000412835.2:n.2077+1G>C
ENST00000635849.1:c.1240+1G>C	ENSP00000490948.1:n.1240+1G>C
ENST00000635957.1:c.874+1G>C	ENSP00000490385.1:n.874+1G>C
ENST00000636930.2:c.3919+1G>C MANE Select	ENSP00000490491.2:n.3919+1G>C
ENST00000636940.1:n.1916+1G>C
ENST00000637015.1:c.1287+1G>C
ENST00000637568.1:c.1201+1G>C
ENST00000637741.1:n.585+1G>C
ENST00000637810.1:c.1261+1G>C	ENSP00000489636.1:n.1261+1G>C
ENST00000637904.1:c.1420+1G>C	ENSP00000490550.1:n.1420+1G>C
ENST00000647938.1:c.3550+1G>C	ENSP00000498155.1:n.3550+1G>C
ENST00000319584.10:c.1936+1G>C	ENSP00000313006.6:n.1936+1G>C
ENST00000346085.9:c.3550+1G>C	ENSP00000344546.4:n.3550+1G>C
ENST00000350026.9:c.3511+1G>C	ENSP00000055163.7:n.3511+1G>C
ENST00000400790.3:c.713G>C	ENSP00000383596.3:p.Gly238Ala
ENST00000414678.6:c.2077+1G>C	ENSP00000412835.2:n.2077+1G>C
NM_017519.2:c.3511+1G>C	NP_059989.2:n.3511+1G>C
NM_020732.3:c.3550+1G>C	NP_065783.3:n.3550+1G>C
XM_005267069.3:c.3670+1G>C	XP_005267126.2:n.3670+1G>C
XM_011535984.1:c.2749+1G>C	XP_011534286.1:n.2749+1G>C
XM_011535985.1:c.2569+1G>C	XP_011534287.1:n.2569+1G>C
XM_011535986.1:c.2329+1G>C	XP_011534288.1:n.2329+1G>C
XM_011535987.1:c.1948+1G>C	XP_011534289.1:n.1948+1G>C
XM_011535988.1:c.811+1G>C	XP_011534290.1:n.811+1G>C
NM_001346813.1:c.3670+1G>C	NP_001333742.1:n.3670+1G>C
NM_001363725.1:c.1420+1G>C	NP_001350654.1:n.1420+1G>C
XM_011535984.2:c.3880+1G>C	XP_011534286.2:n.3880+1G>C
XM_011535988.3:c.811+1G>C	XP_011534290.1:n.811+1G>C
XM_017011103.2:c.3781+1G>C	XP_016866592.1:n.3781+1G>C
XM_017011104.1:c.3751+1G>C	XP_016866593.1:n.3751+1G>C
XM_017011105.2:c.3721+1G>C	XP_016866594.1:n.3721+1G>C
XM_017011106.2:c.3592+1G>C	XP_016866595.1:n.3592+1G>C
XM_017011107.2:c.3571+1G>C	XP_016866596.1:n.3571+1G>C
XR_002956289.1:n.3963+1G>C
NM_001363725.2:c.1420+1G>C	NP_001350654.1:n.1420+1G>C
NM_001371656.1:c.3799+1G>C	NP_001358585.1:n.3799+1G>C
NM_001374820.1:c.3799+1G>C	NP_001361749.1:n.3799+1G>C
NM_001374828.1:c.3919+1G>C MANE Select	NP_001361757.1:n.3919+1G>C
NM_017519.3:c.3760+1G>C	NP_059989.3:n.3760+1G>C