Canonical Allele Identifier: CA366389085

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469980A>C (hg19) ; chr6:g.157148846A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148846A>C , CM000668.2:g.157148846A>C	GRCh38
NC_000006.11:g.157469980A>C , CM000668.1:g.157469980A>C	GRCh37
NC_000006.10:g.157511672A>C	NCBI36
NG_032093.1:g.375917A>C
NG_032093.2:g.375917A>C
NG_066624.1:g.377821A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2984A>C	ENSP00000055163.8:p.Gln995Pro
ENST00000414678.8:c.2894A>C	ENSP00000412835.3:p.Gln965Pro
ENST00000637015.2:c.2984A>C	ENSP00000489729.2:p.Gln995Pro
ENST00000319584.11:c.998A>C	ENSP00000313006.7:p.Gln333Pro
ENST00000346085.10:c.3023A>C	ENSP00000344546.5:p.Gln1008Pro
ENST00000350026.10:c.2735A>C	ENSP00000055163.7:p.Gln912Pro
ENST00000414678.7:c.1142A>C	ENSP00000412835.2:p.Gln381Pro
ENST00000452544.2:n.885A>C
ENST00000635849.1:c.305A>C	ENSP00000490948.1:p.Gln102Pro
ENST00000636426.1:n.118A>C
ENST00000636930.2:c.2984A>C MANE Select	ENSP00000490491.2:p.Gln995Pro
ENST00000637015.1:c.223A>C
ENST00000637568.1:c.27A>C
ENST00000637810.1:c.485A>C	ENSP00000489636.1:p.Gln162Pro
ENST00000637904.1:c.485A>C	ENSP00000490550.1:p.Gln162Pro
ENST00000647938.1:c.2774A>C	ENSP00000498155.1:p.Gln925Pro
ENST00000674190.1:n.1733A>C
ENST00000319584.10:c.1001A>C	ENSP00000313006.6:p.Gln334Pro
ENST00000346085.9:c.2774A>C	ENSP00000344546.4:p.Gln925Pro
ENST00000350026.9:c.2735A>C	ENSP00000055163.7:p.Gln912Pro
ENST00000414678.6:c.1142A>C	ENSP00000412835.2:p.Gln381Pro
ENST00000452544.1:n.831A>C
ENST00000478761.3:c.57A>C
NM_017519.2:c.2735A>C	NP_059989.2:p.Gln912Pro
NM_020732.3:c.2774A>C	NP_065783.3:p.Gln925Pro
XM_005267069.3:c.2735A>C	XP_005267126.2:p.Gln912Pro
XM_011535984.1:c.1685A>C	XP_011534286.1:p.Gln562Pro
XM_011535985.1:c.1505A>C	XP_011534287.1:p.Gln502Pro
XM_011535986.1:c.1265A>C	XP_011534288.1:p.Gln422Pro
XM_011535987.1:c.884A>C	XP_011534289.1:p.Gln295Pro
XM_011535988.1:c.-20+15639A>C	XP_011534290.1:n.-20+15639A>C
NM_001346813.1:c.2735A>C	NP_001333742.1:p.Gln912Pro
NM_001363725.1:c.485A>C	NP_001350654.1:p.Gln162Pro
XM_011535984.2:c.2816A>C	XP_011534286.2:p.Gln939Pro
XM_011535988.3:c.-20+15639A>C	XP_011534290.1:n.-20+15639A>C
XM_017011103.2:c.2816A>C	XP_016866592.1:p.Gln939Pro
XM_017011104.1:c.2816A>C	XP_016866593.1:p.Gln939Pro
XM_017011105.2:c.2816A>C	XP_016866594.1:p.Gln939Pro
XM_017011106.2:c.2816A>C	XP_016866595.1:p.Gln939Pro
XM_017011107.2:c.2636A>C	XP_016866596.1:p.Gln879Pro
XR_002956289.1:n.2899A>C
NM_001363725.2:c.485A>C	NP_001350654.1:p.Gln162Pro
NM_001371656.1:c.3023A>C	NP_001358585.1:p.Gln1008Pro
NM_001374820.1:c.3023A>C	NP_001361749.1:p.Gln1008Pro
NM_001374828.1:c.2984A>C MANE Select	NP_001361757.1:p.Gln995Pro
NM_017519.3:c.2984A>C	NP_059989.3:p.Gln995Pro