Canonical Allele Identifier: CA366389108

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469989G>T (hg19) ; chr6:g.157148855G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148855G>T , CM000668.2:g.157148855G>T	GRCh38
NC_000006.11:g.157469989G>T , CM000668.1:g.157469989G>T	GRCh37
NC_000006.10:g.157511681G>T	NCBI36
NG_032093.1:g.375926G>T
NG_032093.2:g.375926G>T
NG_066624.1:g.377830G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2993G>T	ENSP00000055163.8:p.Gly998Val
ENST00000414678.8:c.2903G>T	ENSP00000412835.3:p.Gly968Val
ENST00000637015.2:c.2993G>T	ENSP00000489729.2:p.Gly998Val
ENST00000319584.11:c.1007G>T	ENSP00000313006.7:p.Gly336Val
ENST00000346085.10:c.3032G>T	ENSP00000344546.5:p.Gly1011Val
ENST00000350026.10:c.2744G>T	ENSP00000055163.7:p.Gly915Val
ENST00000414678.7:c.1151G>T	ENSP00000412835.2:p.Gly384Val
ENST00000452544.2:n.894G>T
ENST00000635849.1:c.314G>T	ENSP00000490948.1:p.Gly105Val
ENST00000636426.1:n.127G>T
ENST00000636930.2:c.2993G>T MANE Select	ENSP00000490491.2:p.Gly998Val
ENST00000637015.1:c.232G>T
ENST00000637568.1:c.36G>T
ENST00000637810.1:c.494G>T	ENSP00000489636.1:p.Gly165Val
ENST00000637904.1:c.494G>T	ENSP00000490550.1:p.Gly165Val
ENST00000647938.1:c.2783G>T	ENSP00000498155.1:p.Gly928Val
ENST00000674190.1:n.1742G>T
ENST00000319584.10:c.1010G>T	ENSP00000313006.6:p.Gly337Val
ENST00000346085.9:c.2783G>T	ENSP00000344546.4:p.Gly928Val
ENST00000350026.9:c.2744G>T	ENSP00000055163.7:p.Gly915Val
ENST00000414678.6:c.1151G>T	ENSP00000412835.2:p.Gly384Val
ENST00000452544.1:n.840G>T
ENST00000478761.3:c.66G>T
NM_017519.2:c.2744G>T	NP_059989.2:p.Gly915Val
NM_020732.3:c.2783G>T	NP_065783.3:p.Gly928Val
XM_005267069.3:c.2744G>T	XP_005267126.2:p.Gly915Val
XM_011535984.1:c.1694G>T	XP_011534286.1:p.Gly565Val
XM_011535985.1:c.1514G>T	XP_011534287.1:p.Gly505Val
XM_011535986.1:c.1274G>T	XP_011534288.1:p.Gly425Val
XM_011535987.1:c.893G>T	XP_011534289.1:p.Gly298Val
XM_011535988.1:c.-20+15648G>T	XP_011534290.1:n.-20+15648G>T
NM_001346813.1:c.2744G>T	NP_001333742.1:p.Gly915Val
NM_001363725.1:c.494G>T	NP_001350654.1:p.Gly165Val
XM_011535984.2:c.2825G>T	XP_011534286.2:p.Gly942Val
XM_011535988.3:c.-20+15648G>T	XP_011534290.1:n.-20+15648G>T
XM_017011103.2:c.2825G>T	XP_016866592.1:p.Gly942Val
XM_017011104.1:c.2825G>T	XP_016866593.1:p.Gly942Val
XM_017011105.2:c.2825G>T	XP_016866594.1:p.Gly942Val
XM_017011106.2:c.2825G>T	XP_016866595.1:p.Gly942Val
XM_017011107.2:c.2645G>T	XP_016866596.1:p.Gly882Val
XR_002956289.1:n.2908G>T
NM_001363725.2:c.494G>T	NP_001350654.1:p.Gly165Val
NM_001371656.1:c.3032G>T	NP_001358585.1:p.Gly1011Val
NM_001374820.1:c.3032G>T	NP_001361749.1:p.Gly1011Val
NM_001374828.1:c.2993G>T MANE Select	NP_001361757.1:p.Gly998Val
NM_017519.3:c.2993G>T	NP_059989.3:p.Gly998Val