Canonical Allele Identifier: CA366242450

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522440A>C (hg19) ; chr6:g.157201306A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201306A>C , CM000668.2:g.157201306A>C	GRCh38
NC_000006.11:g.157522440A>C , CM000668.1:g.157522440A>C	GRCh37
NC_000006.10:g.157564132A>C	NCBI36
NG_032093.1:g.428377A>C
NG_032093.2:g.428377A>C
NG_066624.1:g.430281A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4922A>C	ENSP00000055163.8:p.Lys1641Thr
ENST00000414678.8:c.4991A>C	ENSP00000412835.3:p.Lys1664Thr
ENST00000637015.2:c.5210A>C	ENSP00000489729.2:p.Lys1737Thr
ENST00000346085.10:c.4961A>C	ENSP00000344546.5:p.Lys1654Thr
ENST00000350026.10:c.4673A>C	ENSP00000055163.7:p.Lys1558Thr
ENST00000414678.7:c.3239A>C	ENSP00000412835.2:p.Lys1080Thr
ENST00000635849.1:c.2402A>C	ENSP00000490948.1:p.Lys801Thr
ENST00000635957.1:c.2033A>C	ENSP00000490385.1:p.Lys678Thr
ENST00000636227.1:n.3544A>C
ENST00000636254.1:n.1001A>C
ENST00000636930.2:c.5081A>C MANE Select	ENSP00000490491.2:p.Lys1694Thr
ENST00000636940.1:n.3078A>C
ENST00000637015.1:c.2449A>C
ENST00000637568.1:c.2363A>C
ENST00000637741.1:n.1747A>C
ENST00000637810.1:c.2423A>C	ENSP00000489636.1:p.Lys808Thr
ENST00000637904.1:c.2582A>C	ENSP00000490550.1:p.Lys861Thr
ENST00000647938.1:c.4712A>C	ENSP00000498155.1:p.Lys1571Thr
ENST00000346085.9:c.4712A>C	ENSP00000344546.4:p.Lys1571Thr
ENST00000350026.9:c.4673A>C	ENSP00000055163.7:p.Lys1558Thr
ENST00000414678.6:c.3239A>C	ENSP00000412835.2:p.Lys1080Thr
NM_017519.2:c.4673A>C	NP_059989.2:p.Lys1558Thr
NM_020732.3:c.4712A>C	NP_065783.3:p.Lys1571Thr
XM_005267069.3:c.4832A>C	XP_005267126.2:p.Lys1611Thr
XM_011535984.1:c.3911A>C	XP_011534286.1:p.Lys1304Thr
XM_011535985.1:c.3731A>C	XP_011534287.1:p.Lys1244Thr
XM_011535986.1:c.3491A>C	XP_011534288.1:p.Lys1164Thr
XM_011535987.1:c.3110A>C	XP_011534289.1:p.Lys1037Thr
XM_011535988.1:c.1973A>C	XP_011534290.1:p.Lys658Thr
NM_001346813.1:c.4832A>C	NP_001333742.1:p.Lys1611Thr
NM_001363725.1:c.2582A>C	NP_001350654.1:p.Lys861Thr
XM_011535984.2:c.5042A>C	XP_011534286.2:p.Lys1681Thr
XM_011535988.3:c.1973A>C	XP_011534290.1:p.Lys658Thr
XM_017011103.2:c.4943A>C	XP_016866592.1:p.Lys1648Thr
XM_017011104.1:c.4913A>C	XP_016866593.1:p.Lys1638Thr
XM_017011105.2:c.4883A>C	XP_016866594.1:p.Lys1628Thr
XM_017011106.2:c.4754A>C	XP_016866595.1:p.Lys1585Thr
XM_017011107.2:c.4733A>C	XP_016866596.1:p.Lys1578Thr
XR_002956289.1:n.5028A>C
NM_001363725.2:c.2582A>C	NP_001350654.1:p.Lys861Thr
NM_001371656.1:c.4961A>C	NP_001358585.1:p.Lys1654Thr
NM_001374820.1:c.4961A>C	NP_001361749.1:p.Lys1654Thr
NM_001374828.1:c.5081A>C MANE Select	NP_001361757.1:p.Lys1694Thr
NM_017519.3:c.4922A>C	NP_059989.3:p.Lys1641Thr