Canonical Allele Identifier: CA366234001

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793217001
• MyVariant Identifiers: chr6:g.157510780C>G (hg19) ; chr6:g.157189646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189646C>G , CM000668.2:g.157189646C>G	GRCh38
NC_000006.11:g.157510780C>G , CM000668.1:g.157510780C>G	GRCh37
NC_000006.10:g.157552472C>G	NCBI36
NG_032093.1:g.416717C>G
NG_032093.2:g.416717C>G
NG_066624.1:g.418621C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3765C>G	ENSP00000055163.8:p.Asn1255Lys
ENST00000414678.8:c.3834C>G	ENSP00000412835.3:p.Asn1278Lys
ENST00000637015.2:c.4053C>G	ENSP00000489729.2:p.Asn1351Lys
ENST00000346085.10:c.3804C>G	ENSP00000344546.5:p.Asn1268Lys
ENST00000350026.10:c.3516C>G	ENSP00000055163.7:p.Asn1172Lys
ENST00000414678.7:c.2082C>G	ENSP00000412835.2:p.Asn694Lys
ENST00000635849.1:c.1245C>G	ENSP00000490948.1:p.Asn415Lys
ENST00000635957.1:c.879C>G	ENSP00000490385.1:p.Asn293Lys
ENST00000636930.2:c.3924C>G MANE Select	ENSP00000490491.2:p.Asn1308Lys
ENST00000636940.1:n.1921C>G
ENST00000637015.1:c.1292C>G
ENST00000637568.1:c.1206C>G
ENST00000637741.1:n.590C>G
ENST00000637810.1:c.1266C>G	ENSP00000489636.1:p.Asn422Lys
ENST00000637904.1:c.1425C>G	ENSP00000490550.1:p.Asn475Lys
ENST00000647938.1:c.3555C>G	ENSP00000498155.1:p.Asn1185Lys
ENST00000346085.9:c.3555C>G	ENSP00000344546.4:p.Asn1185Lys
ENST00000350026.9:c.3516C>G	ENSP00000055163.7:p.Asn1172Lys
ENST00000414678.6:c.2082C>G	ENSP00000412835.2:p.Asn694Lys
NM_017519.2:c.3516C>G	NP_059989.2:p.Asn1172Lys
NM_020732.3:c.3555C>G	NP_065783.3:p.Asn1185Lys
XM_005267069.3:c.3675C>G	XP_005267126.2:p.Asn1225Lys
XM_011535984.1:c.2754C>G	XP_011534286.1:p.Asn918Lys
XM_011535985.1:c.2574C>G	XP_011534287.1:p.Asn858Lys
XM_011535986.1:c.2334C>G	XP_011534288.1:p.Asn778Lys
XM_011535987.1:c.1953C>G	XP_011534289.1:p.Asn651Lys
XM_011535988.1:c.816C>G	XP_011534290.1:p.Asn272Lys
NM_001346813.1:c.3675C>G	NP_001333742.1:p.Asn1225Lys
NM_001363725.1:c.1425C>G	NP_001350654.1:p.Asn475Lys
XM_011535984.2:c.3885C>G	XP_011534286.2:p.Asn1295Lys
XM_011535988.3:c.816C>G	XP_011534290.1:p.Asn272Lys
XM_017011103.2:c.3786C>G	XP_016866592.1:p.Asn1262Lys
XM_017011104.1:c.3756C>G	XP_016866593.1:p.Asn1252Lys
XM_017011105.2:c.3726C>G	XP_016866594.1:p.Asn1242Lys
XM_017011106.2:c.3597C>G	XP_016866595.1:p.Asn1199Lys
XM_017011107.2:c.3576C>G	XP_016866596.1:p.Asn1192Lys
XR_002956289.1:n.3968C>G
NM_001363725.2:c.1425C>G	NP_001350654.1:p.Asn475Lys
NM_001371656.1:c.3804C>G	NP_001358585.1:p.Asn1268Lys
NM_001374820.1:c.3804C>G	NP_001361749.1:p.Asn1268Lys
NM_001374828.1:c.3924C>G MANE Select	NP_001361757.1:p.Asn1308Lys
NM_017519.3:c.3765C>G	NP_059989.3:p.Asn1255Lys