Canonical Allele Identifier: CA452978346

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522144T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201010T>C , CM000668.2:g.157201010T>C	GRCh38
NC_000006.11:g.157522144T>C , CM000668.1:g.157522144T>C	GRCh37
NC_000006.10:g.157563836T>C	NCBI36
NG_032093.1:g.428081T>C
NG_032093.2:g.428081T>C
NG_066624.1:g.429985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4626T>C	ENSP00000055163.8:p.Pro1542=
ENST00000414678.8:c.4695T>C	ENSP00000412835.3:p.Pro1565=
ENST00000637015.2:c.4914T>C	ENSP00000489729.2:p.Pro1638=
ENST00000346085.10:c.4665T>C	ENSP00000344546.5:p.Pro1555=
ENST00000350026.10:c.4377T>C	ENSP00000055163.7:p.Pro1459=
ENST00000414678.7:c.2943T>C	ENSP00000412835.2:p.Pro981=
ENST00000635849.1:c.2106T>C	ENSP00000490948.1:p.Pro702=
ENST00000635957.1:c.1737T>C	ENSP00000490385.1:p.Pro579=
ENST00000636227.1:n.3248T>C
ENST00000636254.1:n.705T>C
ENST00000636930.2:c.4785T>C MANE Select	ENSP00000490491.2:p.Pro1595=
ENST00000636940.1:n.2782T>C
ENST00000637015.1:c.2153T>C
ENST00000637568.1:c.2067T>C
ENST00000637741.1:n.1451T>C
ENST00000637810.1:c.2127T>C	ENSP00000489636.1:p.Pro709=
ENST00000637904.1:c.2286T>C	ENSP00000490550.1:p.Pro762=
ENST00000647938.1:c.4416T>C	ENSP00000498155.1:p.Pro1472=
ENST00000346085.9:c.4416T>C	ENSP00000344546.4:p.Pro1472=
ENST00000350026.9:c.4377T>C	ENSP00000055163.7:p.Pro1459=
ENST00000414678.6:c.2943T>C	ENSP00000412835.2:p.Pro981=
NM_017519.2:c.4377T>C	NP_059989.2:p.Pro1459=
NM_020732.3:c.4416T>C	NP_065783.3:p.Pro1472=
XM_005267069.3:c.4536T>C	XP_005267126.2:p.Pro1512=
XM_011535984.1:c.3615T>C	XP_011534286.1:p.Pro1205=
XM_011535985.1:c.3435T>C	XP_011534287.1:p.Pro1145=
XM_011535986.1:c.3195T>C	XP_011534288.1:p.Pro1065=
XM_011535987.1:c.2814T>C	XP_011534289.1:p.Pro938=
XM_011535988.1:c.1677T>C	XP_011534290.1:p.Pro559=
NM_001346813.1:c.4536T>C	NP_001333742.1:p.Pro1512=
NM_001363725.1:c.2286T>C	NP_001350654.1:p.Pro762=
XM_011535984.2:c.4746T>C	XP_011534286.2:p.Pro1582=
XM_011535988.3:c.1677T>C	XP_011534290.1:p.Pro559=
XM_017011103.2:c.4647T>C	XP_016866592.1:p.Pro1549=
XM_017011104.1:c.4617T>C	XP_016866593.1:p.Pro1539=
XM_017011105.2:c.4587T>C	XP_016866594.1:p.Pro1529=
XM_017011106.2:c.4458T>C	XP_016866595.1:p.Pro1486=
XM_017011107.2:c.4437T>C	XP_016866596.1:p.Pro1479=
XR_002956289.1:n.4732T>C
NM_001363725.2:c.2286T>C	NP_001350654.1:p.Pro762=
NM_001371656.1:c.4665T>C	NP_001358585.1:p.Pro1555=
NM_001374820.1:c.4665T>C	NP_001361749.1:p.Pro1555=
NM_001374828.1:c.4785T>C MANE Select	NP_001361757.1:p.Pro1595=
NM_017519.3:c.4626T>C	NP_059989.3:p.Pro1542=