Canonical Allele Identifier: CA366389279

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470071C>A (hg19) ; chr6:g.157148937C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148937C>A , CM000668.2:g.157148937C>A	GRCh38
NC_000006.11:g.157470071C>A , CM000668.1:g.157470071C>A	GRCh37
NC_000006.10:g.157511763C>A	NCBI36
NG_032093.1:g.376008C>A
NG_032093.2:g.376008C>A
NG_066624.1:g.377912C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3075C>A	ENSP00000055163.8:p.Asn1025Lys
ENST00000414678.8:c.2985C>A	ENSP00000412835.3:p.Asn995Lys
ENST00000637015.2:c.3075C>A	ENSP00000489729.2:p.Asn1025Lys
ENST00000319584.11:c.1089C>A	ENSP00000313006.7:p.Asn363Lys
ENST00000346085.10:c.3114C>A	ENSP00000344546.5:p.Asn1038Lys
ENST00000350026.10:c.2826C>A	ENSP00000055163.7:p.Asn942Lys
ENST00000414678.7:c.1233C>A	ENSP00000412835.2:p.Asn411Lys
ENST00000452544.2:n.976C>A
ENST00000635849.1:c.396C>A	ENSP00000490948.1:p.Asn132Lys
ENST00000635957.1:c.30C>A	ENSP00000490385.1:p.Asn10Lys
ENST00000636426.1:n.209C>A
ENST00000636930.2:c.3075C>A MANE Select	ENSP00000490491.2:p.Asn1025Lys
ENST00000637015.1:c.314C>A
ENST00000637568.1:c.118C>A
ENST00000637810.1:c.576C>A	ENSP00000489636.1:p.Asn192Lys
ENST00000637904.1:c.576C>A	ENSP00000490550.1:p.Asn192Lys
ENST00000647938.1:c.2865C>A	ENSP00000498155.1:p.Asn955Lys
ENST00000674190.1:n.1824C>A
ENST00000319584.10:c.1092C>A	ENSP00000313006.6:p.Asn364Lys
ENST00000346085.9:c.2865C>A	ENSP00000344546.4:p.Asn955Lys
ENST00000350026.9:c.2826C>A	ENSP00000055163.7:p.Asn942Lys
ENST00000400790.3:c.27C>A	ENSP00000383596.3:p.Asn9Lys
ENST00000414678.6:c.1233C>A	ENSP00000412835.2:p.Asn411Lys
ENST00000452544.1:n.922C>A
ENST00000478761.3:c.148C>A
NM_017519.2:c.2826C>A	NP_059989.2:p.Asn942Lys
NM_020732.3:c.2865C>A	NP_065783.3:p.Asn955Lys
XM_005267069.3:c.2826C>A	XP_005267126.2:p.Asn942Lys
XM_011535984.1:c.1776C>A	XP_011534286.1:p.Asn592Lys
XM_011535985.1:c.1596C>A	XP_011534287.1:p.Asn532Lys
XM_011535986.1:c.1356C>A	XP_011534288.1:p.Asn452Lys
XM_011535987.1:c.975C>A	XP_011534289.1:p.Asn325Lys
XM_011535988.1:c.-20+15730C>A	XP_011534290.1:n.-20+15730C>A
NM_001346813.1:c.2826C>A	NP_001333742.1:p.Asn942Lys
NM_001363725.1:c.576C>A	NP_001350654.1:p.Asn192Lys
XM_011535984.2:c.2907C>A	XP_011534286.2:p.Asn969Lys
XM_011535988.3:c.-20+15730C>A	XP_011534290.1:n.-20+15730C>A
XM_017011103.2:c.2907C>A	XP_016866592.1:p.Asn969Lys
XM_017011104.1:c.2907C>A	XP_016866593.1:p.Asn969Lys
XM_017011105.2:c.2907C>A	XP_016866594.1:p.Asn969Lys
XM_017011106.2:c.2907C>A	XP_016866595.1:p.Asn969Lys
XM_017011107.2:c.2727C>A	XP_016866596.1:p.Asn909Lys
XR_002956289.1:n.2990C>A
NM_001363725.2:c.576C>A	NP_001350654.1:p.Asn192Lys
NM_001371656.1:c.3114C>A	NP_001358585.1:p.Asn1038Lys
NM_001374820.1:c.3114C>A	NP_001361749.1:p.Asn1038Lys
NM_001374828.1:c.3075C>A MANE Select	NP_001361757.1:p.Asn1025Lys
NM_017519.3:c.3075C>A	NP_059989.3:p.Asn1025Lys