Canonical Allele Identifier: CA366380928

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128211054
• MyVariant Identifiers: chr6:g.157222639C>T (hg19) ; chr6:g.156901505C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901505C>T , CM000668.2:g.156901505C>T	GRCh38
NC_000006.11:g.157222639C>T , CM000668.1:g.157222639C>T	GRCh37
NC_000006.10:g.157264331C>T	NCBI36
NG_032093.1:g.128576C>T
NG_032093.2:g.128576C>T
NG_066624.1:g.130480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2116C>T	ENSP00000055163.8:p.Gln706Ter
ENST00000414678.8:c.2116C>T	ENSP00000412835.3:p.Gln706Ter
ENST00000637015.2:c.2116C>T	ENSP00000489729.2:p.Gln706Ter
ENST00000319584.11:c.130C>T	ENSP00000313006.7:p.Gln44Ter
ENST00000346085.10:c.2155C>T	ENSP00000344546.5:p.Gln719Ter
ENST00000350026.10:c.1867C>T	ENSP00000055163.7:p.Gln623Ter
ENST00000414678.7:c.364C>T	ENSP00000412835.2:p.Gln122Ter
ENST00000636205.1:n.179C>T
ENST00000636748.1:c.397C>T	ENSP00000489917.1:p.Gln133Ter
ENST00000636930.2:c.2116C>T MANE Select	ENSP00000490491.2:p.Gln706Ter
ENST00000637532.1:c.142C>T	ENSP00000490420.1:p.Gln48Ter
ENST00000638000.1:c.333C>T
ENST00000647938.1:c.1906C>T	ENSP00000498155.1:p.Gln636Ter
ENST00000674190.1:n.823C>T
ENST00000674298.1:c.1856C>T
ENST00000319584.10:c.133C>T	ENSP00000313006.6:p.Gln45Ter
ENST00000346085.9:c.1906C>T	ENSP00000344546.4:p.Gln636Ter
ENST00000350026.9:c.1867C>T	ENSP00000055163.7:p.Gln623Ter
ENST00000414678.6:c.364C>T	ENSP00000412835.2:p.Gln122Ter
NM_017519.2:c.1867C>T	NP_059989.2:p.Gln623Ter
NM_020732.3:c.1906C>T	NP_065783.3:p.Gln636Ter
XM_005267069.3:c.1867C>T	XP_005267126.2:p.Gln623Ter
XM_011535984.1:c.775C>T	XP_011534286.1:p.Gln259Ter
XM_011535985.1:c.775C>T	XP_011534287.1:p.Gln259Ter
XM_011535986.1:c.355C>T	XP_011534288.1:p.Gln119Ter
NM_001346813.1:c.1867C>T	NP_001333742.1:p.Gln623Ter
XM_011535984.2:c.1906C>T	XP_011534286.2:p.Gln636Ter
XM_017011103.2:c.1906C>T	XP_016866592.1:p.Gln636Ter
XM_017011104.1:c.1906C>T	XP_016866593.1:p.Gln636Ter
XM_017011105.2:c.1906C>T	XP_016866594.1:p.Gln636Ter
XM_017011106.2:c.1906C>T	XP_016866595.1:p.Gln636Ter
XM_017011107.2:c.1906C>T	XP_016866596.1:p.Gln636Ter
XR_002956289.1:n.1989C>T
NM_001371656.1:c.2155C>T	NP_001358585.1:p.Gln719Ter
NM_001374820.1:c.2155C>T	NP_001361749.1:p.Gln719Ter
NM_001374828.1:c.2116C>T MANE Select	NP_001361757.1:p.Gln706Ter
NM_017519.3:c.2116C>T	NP_059989.3:p.Gln706Ter