Canonical Allele Identifier: CA366389273

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470069A>C (hg19) ; chr6:g.157148935A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148935A>C , CM000668.2:g.157148935A>C	GRCh38
NC_000006.11:g.157470069A>C , CM000668.1:g.157470069A>C	GRCh37
NC_000006.10:g.157511761A>C	NCBI36
NG_032093.1:g.376006A>C
NG_032093.2:g.376006A>C
NG_066624.1:g.377910A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3073A>C	ENSP00000055163.8:p.Asn1025His
ENST00000414678.8:c.2983A>C	ENSP00000412835.3:p.Asn995His
ENST00000637015.2:c.3073A>C	ENSP00000489729.2:p.Asn1025His
ENST00000319584.11:c.1087A>C	ENSP00000313006.7:p.Asn363His
ENST00000346085.10:c.3112A>C	ENSP00000344546.5:p.Asn1038His
ENST00000350026.10:c.2824A>C	ENSP00000055163.7:p.Asn942His
ENST00000414678.7:c.1231A>C	ENSP00000412835.2:p.Asn411His
ENST00000452544.2:n.974A>C
ENST00000635849.1:c.394A>C	ENSP00000490948.1:p.Asn132His
ENST00000635957.1:c.28A>C	ENSP00000490385.1:p.Asn10His
ENST00000636426.1:n.207A>C
ENST00000636930.2:c.3073A>C MANE Select	ENSP00000490491.2:p.Asn1025His
ENST00000637015.1:c.312A>C
ENST00000637568.1:c.116A>C
ENST00000637810.1:c.574A>C	ENSP00000489636.1:p.Asn192His
ENST00000637904.1:c.574A>C	ENSP00000490550.1:p.Asn192His
ENST00000647938.1:c.2863A>C	ENSP00000498155.1:p.Asn955His
ENST00000674190.1:n.1822A>C
ENST00000319584.10:c.1090A>C	ENSP00000313006.6:p.Asn364His
ENST00000346085.9:c.2863A>C	ENSP00000344546.4:p.Asn955His
ENST00000350026.9:c.2824A>C	ENSP00000055163.7:p.Asn942His
ENST00000400790.3:c.25A>C	ENSP00000383596.3:p.Asn9His
ENST00000414678.6:c.1231A>C	ENSP00000412835.2:p.Asn411His
ENST00000452544.1:n.920A>C
ENST00000478761.3:c.146A>C
NM_017519.2:c.2824A>C	NP_059989.2:p.Asn942His
NM_020732.3:c.2863A>C	NP_065783.3:p.Asn955His
XM_005267069.3:c.2824A>C	XP_005267126.2:p.Asn942His
XM_011535984.1:c.1774A>C	XP_011534286.1:p.Asn592His
XM_011535985.1:c.1594A>C	XP_011534287.1:p.Asn532His
XM_011535986.1:c.1354A>C	XP_011534288.1:p.Asn452His
XM_011535987.1:c.973A>C	XP_011534289.1:p.Asn325His
XM_011535988.1:c.-20+15728A>C	XP_011534290.1:n.-20+15728A>C
NM_001346813.1:c.2824A>C	NP_001333742.1:p.Asn942His
NM_001363725.1:c.574A>C	NP_001350654.1:p.Asn192His
XM_011535984.2:c.2905A>C	XP_011534286.2:p.Asn969His
XM_011535988.3:c.-20+15728A>C	XP_011534290.1:n.-20+15728A>C
XM_017011103.2:c.2905A>C	XP_016866592.1:p.Asn969His
XM_017011104.1:c.2905A>C	XP_016866593.1:p.Asn969His
XM_017011105.2:c.2905A>C	XP_016866594.1:p.Asn969His
XM_017011106.2:c.2905A>C	XP_016866595.1:p.Asn969His
XM_017011107.2:c.2725A>C	XP_016866596.1:p.Asn909His
XR_002956289.1:n.2988A>C
NM_001363725.2:c.574A>C	NP_001350654.1:p.Asn192His
NM_001371656.1:c.3112A>C	NP_001358585.1:p.Asn1038His
NM_001374820.1:c.3112A>C	NP_001361749.1:p.Asn1038His
NM_001374828.1:c.3073A>C MANE Select	NP_001361757.1:p.Asn1025His
NM_017519.3:c.3073A>C	NP_059989.3:p.Asn1025His