Canonical Allele Identifier: CA366242026

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522247A>C (hg19) ; chr6:g.157201113A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201113A>C , CM000668.2:g.157201113A>C	GRCh38
NC_000006.11:g.157522247A>C , CM000668.1:g.157522247A>C	GRCh37
NC_000006.10:g.157563939A>C	NCBI36
NG_032093.1:g.428184A>C
NG_032093.2:g.428184A>C
NG_066624.1:g.430088A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4729A>C	ENSP00000055163.8:p.Asn1577His
ENST00000414678.8:c.4798A>C	ENSP00000412835.3:p.Asn1600His
ENST00000637015.2:c.5017A>C	ENSP00000489729.2:p.Asn1673His
ENST00000346085.10:c.4768A>C	ENSP00000344546.5:p.Asn1590His
ENST00000350026.10:c.4480A>C	ENSP00000055163.7:p.Asn1494His
ENST00000414678.7:c.3046A>C	ENSP00000412835.2:p.Asn1016His
ENST00000635849.1:c.2209A>C	ENSP00000490948.1:p.Asn737His
ENST00000635957.1:c.1840A>C	ENSP00000490385.1:p.Asn614His
ENST00000636227.1:n.3351A>C
ENST00000636254.1:n.808A>C
ENST00000636930.2:c.4888A>C MANE Select	ENSP00000490491.2:p.Asn1630His
ENST00000636940.1:n.2885A>C
ENST00000637015.1:c.2256A>C
ENST00000637568.1:c.2170A>C
ENST00000637741.1:n.1554A>C
ENST00000637810.1:c.2230A>C	ENSP00000489636.1:p.Asn744His
ENST00000637904.1:c.2389A>C	ENSP00000490550.1:p.Asn797His
ENST00000647938.1:c.4519A>C	ENSP00000498155.1:p.Asn1507His
ENST00000346085.9:c.4519A>C	ENSP00000344546.4:p.Asn1507His
ENST00000350026.9:c.4480A>C	ENSP00000055163.7:p.Asn1494His
ENST00000414678.6:c.3046A>C	ENSP00000412835.2:p.Asn1016His
NM_017519.2:c.4480A>C	NP_059989.2:p.Asn1494His
NM_020732.3:c.4519A>C	NP_065783.3:p.Asn1507His
XM_005267069.3:c.4639A>C	XP_005267126.2:p.Asn1547His
XM_011535984.1:c.3718A>C	XP_011534286.1:p.Asn1240His
XM_011535985.1:c.3538A>C	XP_011534287.1:p.Asn1180His
XM_011535986.1:c.3298A>C	XP_011534288.1:p.Asn1100His
XM_011535987.1:c.2917A>C	XP_011534289.1:p.Asn973His
XM_011535988.1:c.1780A>C	XP_011534290.1:p.Asn594His
NM_001346813.1:c.4639A>C	NP_001333742.1:p.Asn1547His
NM_001363725.1:c.2389A>C	NP_001350654.1:p.Asn797His
XM_011535984.2:c.4849A>C	XP_011534286.2:p.Asn1617His
XM_011535988.3:c.1780A>C	XP_011534290.1:p.Asn594His
XM_017011103.2:c.4750A>C	XP_016866592.1:p.Asn1584His
XM_017011104.1:c.4720A>C	XP_016866593.1:p.Asn1574His
XM_017011105.2:c.4690A>C	XP_016866594.1:p.Asn1564His
XM_017011106.2:c.4561A>C	XP_016866595.1:p.Asn1521His
XM_017011107.2:c.4540A>C	XP_016866596.1:p.Asn1514His
XR_002956289.1:n.4835A>C
NM_001363725.2:c.2389A>C	NP_001350654.1:p.Asn797His
NM_001371656.1:c.4768A>C	NP_001358585.1:p.Asn1590His
NM_001374820.1:c.4768A>C	NP_001361749.1:p.Asn1590His
NM_001374828.1:c.4888A>C MANE Select	NP_001361757.1:p.Asn1630His
NM_017519.3:c.4729A>C	NP_059989.3:p.Asn1577His