Canonical Allele Identifier: CA366389185

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554226126
• MyVariant Identifiers: chr6:g.157470027A>T (hg19) ; chr6:g.157148893A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148893A>T , CM000668.2:g.157148893A>T	GRCh38
NC_000006.11:g.157470027A>T , CM000668.1:g.157470027A>T	GRCh37
NC_000006.10:g.157511719A>T	NCBI36
NG_032093.1:g.375964A>T
NG_032093.2:g.375964A>T
NG_066624.1:g.377868A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3031A>T	ENSP00000055163.8:p.Lys1011Ter
ENST00000414678.8:c.2941A>T	ENSP00000412835.3:p.Lys981Ter
ENST00000637015.2:c.3031A>T	ENSP00000489729.2:p.Lys1011Ter
ENST00000319584.11:c.1045A>T	ENSP00000313006.7:p.Lys349Ter
ENST00000346085.10:c.3070A>T	ENSP00000344546.5:p.Lys1024Ter
ENST00000350026.10:c.2782A>T	ENSP00000055163.7:p.Lys928Ter
ENST00000414678.7:c.1189A>T	ENSP00000412835.2:p.Lys397Ter
ENST00000452544.2:n.932A>T
ENST00000635849.1:c.352A>T	ENSP00000490948.1:p.Lys118Ter
ENST00000636426.1:n.165A>T
ENST00000636930.2:c.3031A>T MANE Select	ENSP00000490491.2:p.Lys1011Ter
ENST00000637015.1:c.270A>T
ENST00000637568.1:c.74A>T
ENST00000637810.1:c.532A>T	ENSP00000489636.1:p.Lys178Ter
ENST00000637904.1:c.532A>T	ENSP00000490550.1:p.Lys178Ter
ENST00000647938.1:c.2821A>T	ENSP00000498155.1:p.Lys941Ter
ENST00000674190.1:n.1780A>T
ENST00000319584.10:c.1048A>T	ENSP00000313006.6:p.Lys350Ter
ENST00000346085.9:c.2821A>T	ENSP00000344546.4:p.Lys941Ter
ENST00000350026.9:c.2782A>T	ENSP00000055163.7:p.Lys928Ter
ENST00000414678.6:c.1189A>T	ENSP00000412835.2:p.Lys397Ter
ENST00000452544.1:n.878A>T
ENST00000478761.3:c.104A>T
NM_017519.2:c.2782A>T	NP_059989.2:p.Lys928Ter
NM_020732.3:c.2821A>T	NP_065783.3:p.Lys941Ter
XM_005267069.3:c.2782A>T	XP_005267126.2:p.Lys928Ter
XM_011535984.1:c.1732A>T	XP_011534286.1:p.Lys578Ter
XM_011535985.1:c.1552A>T	XP_011534287.1:p.Lys518Ter
XM_011535986.1:c.1312A>T	XP_011534288.1:p.Lys438Ter
XM_011535987.1:c.931A>T	XP_011534289.1:p.Lys311Ter
XM_011535988.1:c.-20+15686A>T	XP_011534290.1:n.-20+15686A>T
NM_001346813.1:c.2782A>T	NP_001333742.1:p.Lys928Ter
NM_001363725.1:c.532A>T	NP_001350654.1:p.Lys178Ter
XM_011535984.2:c.2863A>T	XP_011534286.2:p.Lys955Ter
XM_011535988.3:c.-20+15686A>T	XP_011534290.1:n.-20+15686A>T
XM_017011103.2:c.2863A>T	XP_016866592.1:p.Lys955Ter
XM_017011104.1:c.2863A>T	XP_016866593.1:p.Lys955Ter
XM_017011105.2:c.2863A>T	XP_016866594.1:p.Lys955Ter
XM_017011106.2:c.2863A>T	XP_016866595.1:p.Lys955Ter
XM_017011107.2:c.2683A>T	XP_016866596.1:p.Lys895Ter
XR_002956289.1:n.2946A>T
NM_001363725.2:c.532A>T	NP_001350654.1:p.Lys178Ter
NM_001371656.1:c.3070A>T	NP_001358585.1:p.Lys1024Ter
NM_001374820.1:c.3070A>T	NP_001361749.1:p.Lys1024Ter
NM_001374828.1:c.3031A>T MANE Select	NP_001361757.1:p.Lys1011Ter
NM_017519.3:c.3031A>T	NP_059989.3:p.Lys1011Ter