Canonical Allele Identifier: CA366384017

Gene: ARID1B

Linked Data

• dbSNP Id: rs1057518951
• MyVariant Identifiers: chr6:g.157150430C>G (hg19) ; chr6:g.156829296C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829296C>G , CM000668.2:g.156829296C>G	GRCh38
NC_000006.11:g.157150430C>G , CM000668.1:g.157150430C>G	GRCh37
NC_000006.10:g.157192122C>G	NCBI36
NG_032093.1:g.56367C>G
NG_032093.2:g.56367C>G
NG_066624.1:g.58271C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.1861C>G	ENSP00000055163.8:p.Gln621Glu
ENST00000414678.8:c.1861C>G	ENSP00000412835.3:p.Gln621Glu
ENST00000637015.2:c.1861C>G	ENSP00000489729.2:p.Gln621Glu
ENST00000346085.10:c.1861C>G	ENSP00000344546.5:p.Gln621Glu
ENST00000350026.10:c.1612C>G	ENSP00000055163.7:p.Gln538Glu
ENST00000414678.7:c.109C>G	ENSP00000412835.2:p.Gln37Glu
ENST00000494260.2:c.142C>G	ENSP00000490094.1:p.Gln48Glu
ENST00000636607.1:c.124C>G	ENSP00000490050.1:p.Gln42Glu
ENST00000636748.1:c.142C>G	ENSP00000489917.1:p.Gln48Glu
ENST00000636930.2:c.1861C>G MANE Select	ENSP00000490491.2:p.Gln621Glu
ENST00000637910.1:n.142C>G
ENST00000638000.1:c.78C>G
ENST00000647938.1:c.1612C>G	ENSP00000498155.1:p.Gln538Glu
ENST00000674190.1:n.568C>G
ENST00000674298.1:c.1601C>G
ENST00000346085.9:c.1612C>G	ENSP00000344546.4:p.Gln538Glu
ENST00000350026.9:c.1612C>G	ENSP00000055163.7:p.Gln538Glu
ENST00000414678.6:c.109C>G	ENSP00000412835.2:p.Gln37Glu
ENST00000494260.1:n.70C>G
NM_017519.2:c.1612C>G	NP_059989.2:p.Gln538Glu
NM_020732.3:c.1612C>G	NP_065783.3:p.Gln538Glu
XM_005267069.3:c.1612C>G	XP_005267126.2:p.Gln538Glu
XM_011535984.1:c.481C>G	XP_011534286.1:p.Gln161Glu
XM_011535985.1:c.481C>G	XP_011534287.1:p.Gln161Glu
XM_011535986.1:c.61C>G	XP_011534288.1:p.Gln21Glu
NM_001346813.1:c.1612C>G	NP_001333742.1:p.Gln538Glu
XM_011535984.2:c.1612C>G	XP_011534286.2:p.Gln538Glu
XM_017011103.2:c.1612C>G	XP_016866592.1:p.Gln538Glu
XM_017011104.1:c.1612C>G	XP_016866593.1:p.Gln538Glu
XM_017011105.2:c.1612C>G	XP_016866594.1:p.Gln538Glu
XM_017011106.2:c.1612C>G	XP_016866595.1:p.Gln538Glu
XM_017011107.2:c.1612C>G	XP_016866596.1:p.Gln538Glu
XR_002956289.1:n.1695C>G
NM_001371656.1:c.1861C>G	NP_001358585.1:p.Gln621Glu
NM_001374820.1:c.1861C>G	NP_001361749.1:p.Gln621Glu
NM_001374828.1:c.1861C>G MANE Select	NP_001361757.1:p.Gln621Glu
NM_017519.3:c.1861C>G	NP_059989.3:p.Gln621Glu